Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.117591251_117595608delinsCTACATTTGTACTA | CA2580076490 | CFTR | c.1767-683_2619+550delinsCTACATTTGTACTA c.*1481-683_*2333+550delinsCTACATTTGTACTA c.1584-683_2436+550delinsCTACATTTGTACTA c.*67-683_*919+550delinsCTACATTTGTACTA c.*1591-683_*2443+550delinsCTACATTTGTACTA c.1341-683_2193+550delinsCTACATTTGTACTA c.1402-11575_1402-7218delinsCTACATTTGTACTA (n.1402-11575_1402-7218delinsCTACATTTGTACTA) c.1677-683_2529+550delinsCTACATTTGTACTA c.1857-683_2709+550delinsCTACATTTGTACTA c.1524-683_2376+550delinsCTACATTTGTACTA | ClinVar |
7 | g.117592380T>A | CA368980432 | CFTR | c.2213T>A (p.Leu738Ter) c.*1927T>A (n.*1927T>A) c.2030T>A (p.Leu677Ter) c.*513T>A (n.*513T>A) c.*2037T>A (n.*2037T>A) c.1787T>A (p.Leu596Ter) c.1402-10446T>A (n.1402-10446T>A) c.2123T>A (p.Leu708Ter) c.2303T>A (p.Leu768Ter) c.1970T>A (p.Leu657Ter) | |
7 | g.117592380T>C | CA368980428 | CFTR | c.2213T>C (p.Leu738Ser) c.*1927T>C (n.*1927T>C) c.2030T>C (p.Leu677Ser) c.*513T>C (n.*513T>C) c.*2037T>C (n.*2037T>C) c.1787T>C (p.Leu596Ser) c.1402-10446T>C (n.1402-10446T>C) c.2123T>C (p.Leu708Ser) c.2303T>C (p.Leu768Ser) c.1970T>C (p.Leu657Ser) | |
7 | g.117592380T>G | CA368980429 | CFTR | c.2213T>G (p.Leu738Ter) c.*1927T>G (n.*1927T>G) c.2030T>G (p.Leu677Ter) c.*513T>G (n.*513T>G) c.*2037T>G (n.*2037T>G) c.1787T>G (p.Leu596Ter) c.1402-10446T>G (n.1402-10446T>G) c.2123T>G (p.Leu708Ter) c.2303T>G (p.Leu768Ter) c.1970T>G (p.Leu657Ter) | ClinVar |
7 | g.117592381A= | CA1737395023 | CFTR | c.2214A= (p.Leu738=) c.*1928A= (n.*1928A=) c.2031A= (p.Leu677=) c.*514A= (n.*514A=) c.*2038A= (n.*2038A=) c.1788A= (p.Leu596=) c.1402-10445A= (n.1402-10445A=) c.2124A= (p.Leu708=) c.2304A= (p.Leu768=) c.1971A= (p.Leu657=) | |
7 | g.117592381A>C | CA368980434 | CFTR | c.2214A>C (p.Leu738Phe) c.*1928A>C (n.*1928A>C) c.2031A>C (p.Leu677Phe) c.*514A>C (n.*514A>C) c.*2038A>C (n.*2038A>C) c.1788A>C (p.Leu596Phe) c.1402-10445A>C (n.1402-10445A>C) c.2124A>C (p.Leu708Phe) c.2304A>C (p.Leu768Phe) c.1971A>C (p.Leu657Phe) | dbSNP |
7 | g.117592381A>G | CA457449456 | CFTR | c.2214A>G (p.Leu738=) c.*1928A>G (n.*1928A>G) c.2031A>G (p.Leu677=) c.*514A>G (n.*514A>G) c.*2038A>G (n.*2038A>G) c.1788A>G (p.Leu596=) c.1402-10445A>G (n.1402-10445A>G) c.2124A>G (p.Leu708=) c.2304A>G (p.Leu768=) c.1971A>G (p.Leu657=) | |
7 | g.117592381A>T | CA368980436 | CFTR | c.2214A>T (p.Leu738Phe) c.*1928A>T (n.*1928A>T) c.2031A>T (p.Leu677Phe) c.*514A>T (n.*514A>T) c.*2038A>T (n.*2038A>T) c.1788A>T (p.Leu596Phe) c.1402-10445A>T (n.1402-10445A>T) c.2124A>T (p.Leu708Phe) c.2304A>T (p.Leu768Phe) c.1971A>T (p.Leu657Phe) | gnomAD v4 |
7 | g.117592381_117592382delinsAG | CA1737395021 | CFTR | c.2214_2215delinsAG (p.Leu738=) c.*1928_*1929delinsAG (n.*1928_*1929delinsAG) c.2031_2032delinsAG (p.Leu677=) c.*514_*515delinsAG (n.*514_*515delinsAG) c.*2038_*2039delinsAG (n.*2038_*2039delinsAG) c.1788_1789delinsAG (p.Leu596=) c.1402-10445_1402-10444delinsAG (n.1402-10445_1402-10444delinsAG) c.2124_2125delinsAG (p.Leu708=) c.2304_2305delinsAG (p.Leu768=) c.1971_1972delinsAG (p.Leu657=) | |
7 | g.117592382del | CA328097 | CFTR | c.2215del (p.Val739TyrfsTer16) c.*1929del (n.*1929del) c.2032del (p.Val678TyrfsTer16) c.*515del (n.*515del) c.*2039del (n.*2039del) c.1789del (p.Val597TyrfsTer16) c.1402-10444del (n.1402-10444del) c.2125del (p.Val709TyrfsTer16) c.2305del (p.Val769TyrfsTer16) c.1972del (p.Val658TyrfsTer16) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.117592382G>A | CA4451154 | CFTR | c.2215G>A (p.Val739Ile) c.*1929G>A (n.*1929G>A) c.2032G>A (p.Val678Ile) c.*515G>A (n.*515G>A) c.*2039G>A (n.*2039G>A) c.1789G>A (p.Val597Ile) c.1402-10444G>A (n.1402-10444G>A) c.2125G>A (p.Val709Ile) c.2305G>A (p.Val769Ile) c.1972G>A (p.Val658Ile) | dbSNP ExAC gnomAD v3 gnomAD v4 |
7 | g.117592382G>C | CA368980440 | CFTR | c.2215G>C (p.Val739Leu) c.*1929G>C (n.*1929G>C) c.2032G>C (p.Val678Leu) c.*515G>C (n.*515G>C) c.*2039G>C (n.*2039G>C) c.1789G>C (p.Val597Leu) c.1402-10444G>C (n.1402-10444G>C) c.2125G>C (p.Val709Leu) c.2305G>C (p.Val769Leu) c.1972G>C (p.Val658Leu) | gnomAD v4 |
7 | g.117592382G= | CA1737395030 | CFTR | c.2215G= (p.Val739=) c.*1929G= (n.*1929G=) c.2032G= (p.Val678=) c.*515G= (n.*515G=) c.*2039G= (n.*2039G=) c.1789G= (p.Val597=) c.1402-10444G= (n.1402-10444G=) c.2125G= (p.Val709=) c.2305G= (p.Val769=) c.1972G= (p.Val658=) | |
7 | g.117592382G>T | CA368980442 | CFTR | c.2215G>T (p.Val739Leu) c.*1929G>T (n.*1929G>T) c.2032G>T (p.Val678Leu) c.*515G>T (n.*515G>T) c.*2039G>T (n.*2039G>T) c.1789G>T (p.Val597Leu) c.1402-10444G>T (n.1402-10444G>T) c.2125G>T (p.Val709Leu) c.2305G>T (p.Val769Leu) c.1972G>T (p.Val658Leu) | |
7 | g.117592383T>A | CA368980446 | CFTR | c.2216T>A (p.Val739Glu) c.*1930T>A (n.*1930T>A) c.2033T>A (p.Val678Glu) c.*516T>A (n.*516T>A) c.*2040T>A (n.*2040T>A) c.1790T>A (p.Val597Glu) c.1402-10443T>A (n.1402-10443T>A) c.2126T>A (p.Val709Glu) c.2306T>A (p.Val769Glu) c.1973T>A (p.Val658Glu) | |
7 | g.117592383T>C | CA368980448 | CFTR | c.2216T>C (p.Val739Ala) c.*1930T>C (n.*1930T>C) c.2033T>C (p.Val678Ala) c.*516T>C (n.*516T>C) c.*2040T>C (n.*2040T>C) c.1790T>C (p.Val597Ala) c.1402-10443T>C (n.1402-10443T>C) c.2126T>C (p.Val709Ala) c.2306T>C (p.Val769Ala) c.1973T>C (p.Val658Ala) | gnomAD v4 |
7 | g.117592383T>G | CA368980451 | CFTR | c.2216T>G (p.Val739Gly) c.*1930T>G (n.*1930T>G) c.2033T>G (p.Val678Gly) c.*516T>G (n.*516T>G) c.*2040T>G (n.*2040T>G) c.1790T>G (p.Val597Gly) c.1402-10443T>G (n.1402-10443T>G) c.2126T>G (p.Val709Gly) c.2306T>G (p.Val769Gly) c.1973T>G (p.Val658Gly) | gnomAD v4 |
7 | g.117592384A>C | CA457449464 | CFTR | c.2217A>C (p.Val739=) c.*1931A>C (n.*1931A>C) c.2034A>C (p.Val678=) c.*517A>C (n.*517A>C) c.*2041A>C (n.*2041A>C) c.1791A>C (p.Val597=) c.1402-10442A>C (n.1402-10442A>C) c.2127A>C (p.Val709=) c.2307A>C (p.Val769=) c.1974A>C (p.Val658=) | |
7 | g.117592384A>G | CA457449465 | CFTR | c.2217A>G (p.Val739=) c.*1931A>G (n.*1931A>G) c.2034A>G (p.Val678=) c.*517A>G (n.*517A>G) c.*2041A>G (n.*2041A>G) c.1791A>G (p.Val597=) c.1402-10442A>G (n.1402-10442A>G) c.2127A>G (p.Val709=) c.2307A>G (p.Val769=) c.1974A>G (p.Val658=) | ClinVar |
7 | g.117592384A>T | CA457449466 | CFTR | c.2217A>T (p.Val739=) c.*1931A>T (n.*1931A>T) c.2034A>T (p.Val678=) c.*517A>T (n.*517A>T) c.*2041A>T (n.*2041A>T) c.1791A>T (p.Val597=) c.1402-10442A>T (n.1402-10442A>T) c.2127A>T (p.Val709=) c.2307A>T (p.Val769=) c.1974A>T (p.Val658=) | |
7 | g.117592385C>A | CA368980454 | CFTR | c.2218C>A (p.Pro740Thr) c.*1932C>A (n.*1932C>A) c.2035C>A (p.Pro679Thr) c.*518C>A (n.*518C>A) c.*2042C>A (n.*2042C>A) c.1792C>A (p.Pro598Thr) c.1402-10441C>A (n.1402-10441C>A) c.2128C>A (p.Pro710Thr) c.2308C>A (p.Pro770Thr) c.1975C>A (p.Pro659Thr) | |
7 | g.117592385C>G | CA368980456 | CFTR | c.2218C>G (p.Pro740Ala) c.*1932C>G (n.*1932C>G) c.2035C>G (p.Pro679Ala) c.*518C>G (n.*518C>G) c.*2042C>G (n.*2042C>G) c.1792C>G (p.Pro598Ala) c.1402-10441C>G (n.1402-10441C>G) c.2128C>G (p.Pro710Ala) c.2308C>G (p.Pro770Ala) c.1975C>G (p.Pro659Ala) | |
7 | g.117592385C>T | CA368980459 | CFTR | c.2218C>T (p.Pro740Ser) c.*1932C>T (n.*1932C>T) c.2035C>T (p.Pro679Ser) c.*518C>T (n.*518C>T) c.*2042C>T (n.*2042C>T) c.1792C>T (p.Pro598Ser) c.1402-10441C>T (n.1402-10441C>T) c.2128C>T (p.Pro710Ser) c.2308C>T (p.Pro770Ser) c.1975C>T (p.Pro659Ser) | |
7 | g.117592385_117592386insAATGGAAAATTTT | CA2507749182 | CFTR | c.2218_2219insAATGGAAAATTTT (p.Pro740GlnfsTer8) c.*1932_*1933insAATGGAAAATTTT (n.*1932_*1933insAATGGAAAATTTT) c.2035_2036insAATGGAAAATTTT (p.Pro679GlnfsTer8) c.*518_*519insAATGGAAAATTTT (n.*518_*519insAATGGAAAATTTT) c.*2042_*2043insAATGGAAAATTTT (n.*2042_*2043insAATGGAAAATTTT) c.1792_1793insAATGGAAAATTTT (p.Pro598GlnfsTer8) c.1402-10441_1402-10440insAATGGAAAATTTT (n.1402-10441_1402-10440insAATGGAAAATTTT) c.2128_2129insAATGGAAAATTTT (p.Pro710GlnfsTer8) c.2308_2309insAATGGAAAATTTT (p.Pro770GlnfsTer8) c.1975_1976insAATGGAAAATTTT (p.Pro659GlnfsTer8) | |
7 | g.117592386C>A | CA368980466 | CFTR | c.2219C>A (p.Pro740Gln) c.*1933C>A (n.*1933C>A) c.2036C>A (p.Pro679Gln) c.*519C>A (n.*519C>A) c.*2043C>A (n.*2043C>A) c.1793C>A (p.Pro598Gln) c.1402-10440C>A (n.1402-10440C>A) c.2129C>A (p.Pro710Gln) c.2309C>A (p.Pro770Gln) c.1976C>A (p.Pro659Gln) | dbSNP |
7 | g.117592386C= | CA1737395036 | CFTR | c.2219C= (p.Pro740=) c.*1933C= (n.*1933C=) c.2036C= (p.Pro679=) c.*519C= (n.*519C=) c.*2043C= (n.*2043C=) c.1793C= (p.Pro598=) c.1402-10440C= (n.1402-10440C=) c.2129C= (p.Pro710=) c.2309C= (p.Pro770=) c.1976C= (p.Pro659=) | |
7 | g.117592386C>G | CA368980464 | CFTR | c.2219C>G (p.Pro740Arg) c.*1933C>G (n.*1933C>G) c.2036C>G (p.Pro679Arg) c.*519C>G (n.*519C>G) c.*2043C>G (n.*2043C>G) c.1793C>G (p.Pro598Arg) c.1402-10440C>G (n.1402-10440C>G) c.2129C>G (p.Pro710Arg) c.2309C>G (p.Pro770Arg) c.1976C>G (p.Pro659Arg) | gnomAD v4 |
7 | g.117592386C>T | CA4451155 | CFTR | c.2219C>T (p.Pro740Leu) c.*1933C>T (n.*1933C>T) c.2036C>T (p.Pro679Leu) c.*519C>T (n.*519C>T) c.*2043C>T (n.*2043C>T) c.1793C>T (p.Pro598Leu) c.1402-10440C>T (n.1402-10440C>T) c.2129C>T (p.Pro710Leu) c.2309C>T (p.Pro770Leu) c.1976C>T (p.Pro659Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.117592386_117592387insGTATAGAGTTGATTGGATTG | CA2570260356 | CFTR | c.2219_2220insGTATAGAGTTGATTGGATTG (p.Asp741TyrfsTer21) c.*1933_*1934insGTATAGAGTTGATTGGATTG (n.*1933_*1934insGTATAGAGTTGATTGGATTG) c.2036_2037insGTATAGAGTTGATTGGATTG (p.Asp680TyrfsTer21) c.*519_*520insGTATAGAGTTGATTGGATTG (n.*519_*520insGTATAGAGTTGATTGGATTG) c.*2043_*2044insGTATAGAGTTGATTGGATTG (n.*2043_*2044insGTATAGAGTTGATTGGATTG) c.1793_1794insGTATAGAGTTGATTGGATTG (p.Asp599TyrfsTer21) c.1402-10440_1402-10439insGTATAGAGTTGATTGGATTG (n.1402-10440_1402-10439insGTATAGAGTTGATTGGATTG) c.2129_2130insGTATAGAGTTGATTGGATTG (p.Asp711TyrfsTer21) c.2309_2310insGTATAGAGTTGATTGGATTG (p.Asp771TyrfsTer21) c.1976_1977insGTATAGAGTTGATTGGATTG (p.Asp660TyrfsTer21) | |
7 | g.117592387A= | CA1737395043 | CFTR | c.2220A= (p.Pro740=) c.*1934A= (n.*1934A=) c.2037A= (p.Pro679=) c.*520A= (n.*520A=) c.*2044A= (n.*2044A=) c.1794A= (p.Pro598=) c.1402-10439A= (n.1402-10439A=) c.2130A= (p.Pro710=) c.2310A= (p.Pro770=) c.1977A= (p.Pro659=) | |
7 | g.117592387A>C | CA457449471 | CFTR | c.2220A>C (p.Pro740=) c.*1934A>C (n.*1934A>C) c.2037A>C (p.Pro679=) c.*520A>C (n.*520A>C) c.*2044A>C (n.*2044A>C) c.1794A>C (p.Pro598=) c.1402-10439A>C (n.1402-10439A>C) c.2130A>C (p.Pro710=) c.2310A>C (p.Pro770=) c.1977A>C (p.Pro659=) | |
7 | g.117592387A>G | CA457449473 | CFTR | c.2220A>G (p.Pro740=) c.*1934A>G (n.*1934A>G) c.2037A>G (p.Pro679=) c.*520A>G (n.*520A>G) c.*2044A>G (n.*2044A>G) c.1794A>G (p.Pro598=) c.1402-10439A>G (n.1402-10439A>G) c.2130A>G (p.Pro710=) c.2310A>G (p.Pro770=) c.1977A>G (p.Pro659=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
7 | g.117592387A>T | CA457449472 | CFTR | c.2220A>T (p.Pro740=) c.*1934A>T (n.*1934A>T) c.2037A>T (p.Pro679=) c.*520A>T (n.*520A>T) c.*2044A>T (n.*2044A>T) c.1794A>T (p.Pro598=) c.1402-10439A>T (n.1402-10439A>T) c.2130A>T (p.Pro710=) c.2310A>T (p.Pro770=) c.1977A>T (p.Pro659=) | |
7 | g.117592388G>A | CA368980468 | CFTR | c.2221G>A (p.Asp741Asn) c.*1935G>A (n.*1935G>A) c.2038G>A (p.Asp680Asn) c.*521G>A (n.*521G>A) c.*2045G>A (n.*2045G>A) c.1795G>A (p.Asp599Asn) c.1402-10438G>A (n.1402-10438G>A) c.2131G>A (p.Asp711Asn) c.2311G>A (p.Asp771Asn) c.1978G>A (p.Asp660Asn) | |
7 | g.117592388G>C | CA368980467 | CFTR | c.2221G>C (p.Asp741His) c.*1935G>C (n.*1935G>C) c.2038G>C (p.Asp680His) c.*521G>C (n.*521G>C) c.*2045G>C (n.*2045G>C) c.1795G>C (p.Asp599His) c.1402-10438G>C (n.1402-10438G>C) c.2131G>C (p.Asp711His) c.2311G>C (p.Asp771His) c.1978G>C (p.Asp660His) | |
7 | g.117592388G>T | CA368980470 | CFTR | c.2221G>T (p.Asp741Tyr) c.*1935G>T (n.*1935G>T) c.2038G>T (p.Asp680Tyr) c.*521G>T (n.*521G>T) c.*2045G>T (n.*2045G>T) c.1795G>T (p.Asp599Tyr) c.1402-10438G>T (n.1402-10438G>T) c.2131G>T (p.Asp711Tyr) c.2311G>T (p.Asp771Tyr) c.1978G>T (p.Asp660Tyr) | gnomAD v4 |
7 | g.117592389A>C | CA368980473 | CFTR | c.2222A>C (p.Asp741Ala) c.*1936A>C (n.*1936A>C) c.2039A>C (p.Asp680Ala) c.*522A>C (n.*522A>C) c.*2046A>C (n.*2046A>C) c.1796A>C (p.Asp599Ala) c.1402-10437A>C (n.1402-10437A>C) c.2132A>C (p.Asp711Ala) c.2312A>C (p.Asp771Ala) c.1979A>C (p.Asp660Ala) | |
7 | g.117592389A>G | CA368980474 | CFTR | c.2222A>G (p.Asp741Gly) c.*1936A>G (n.*1936A>G) c.2039A>G (p.Asp680Gly) c.*522A>G (n.*522A>G) c.*2046A>G (n.*2046A>G) c.1796A>G (p.Asp599Gly) c.1402-10437A>G (n.1402-10437A>G) c.2132A>G (p.Asp711Gly) c.2312A>G (p.Asp771Gly) c.1979A>G (p.Asp660Gly) | |
7 | g.117592389A>T | CA368980477 | CFTR | c.2222A>T (p.Asp741Val) c.*1936A>T (n.*1936A>T) c.2039A>T (p.Asp680Val) c.*522A>T (n.*522A>T) c.*2046A>T (n.*2046A>T) c.1796A>T (p.Asp599Val) c.1402-10437A>T (n.1402-10437A>T) c.2132A>T (p.Asp711Val) c.2312A>T (p.Asp771Val) c.1979A>T (p.Asp660Val) | |
7 | g.117592390T>A | CA368980479 | CFTR | c.2223T>A (p.Asp741Glu) c.*1937T>A (n.*1937T>A) c.2040T>A (p.Asp680Glu) c.*523T>A (n.*523T>A) c.*2047T>A (n.*2047T>A) c.1797T>A (p.Asp599Glu) c.1402-10436T>A (n.1402-10436T>A) c.2133T>A (p.Asp711Glu) c.2313T>A (p.Asp771Glu) c.1980T>A (p.Asp660Glu) | |
7 | g.117592390T>C | CA457449481 | CFTR | c.2223T>C (p.Asp741=) c.*1937T>C (n.*1937T>C) c.2040T>C (p.Asp680=) c.*523T>C (n.*523T>C) c.*2047T>C (n.*2047T>C) c.1797T>C (p.Asp599=) c.1402-10436T>C (n.1402-10436T>C) c.2133T>C (p.Asp711=) c.2313T>C (p.Asp771=) c.1980T>C (p.Asp660=) | gnomAD v4 |
7 | g.117592390T>G | CA368980480 | CFTR | c.2223T>G (p.Asp741Glu) c.*1937T>G (n.*1937T>G) c.2040T>G (p.Asp680Glu) c.*523T>G (n.*523T>G) c.*2047T>G (n.*2047T>G) c.1797T>G (p.Asp599Glu) c.1402-10436T>G (n.1402-10436T>G) c.2133T>G (p.Asp711Glu) c.2313T>G (p.Asp771Glu) c.1980T>G (p.Asp660Glu) | |
7 | g.117592391T>A | CA368980485 | CFTR | c.2224T>A (p.Ser742Thr) c.*1938T>A (n.*1938T>A) c.2041T>A (p.Ser681Thr) c.*524T>A (n.*524T>A) c.*2048T>A (n.*2048T>A) c.1798T>A (p.Ser600Thr) c.1402-10435T>A (n.1402-10435T>A) c.2134T>A (p.Ser712Thr) c.2314T>A (p.Ser772Thr) c.1981T>A (p.Ser661Thr) | |
7 | g.117592391T>C | CA368980482 | CFTR | c.2224T>C (p.Ser742Pro) c.*1938T>C (n.*1938T>C) c.2041T>C (p.Ser681Pro) c.*524T>C (n.*524T>C) c.*2048T>C (n.*2048T>C) c.1798T>C (p.Ser600Pro) c.1402-10435T>C (n.1402-10435T>C) c.2134T>C (p.Ser712Pro) c.2314T>C (p.Ser772Pro) c.1981T>C (p.Ser661Pro) | |
7 | g.117592391T>G | CA368980481 | CFTR | c.2224T>G (p.Ser742Ala) c.*1938T>G (n.*1938T>G) c.2041T>G (p.Ser681Ala) c.*524T>G (n.*524T>G) c.*2048T>G (n.*2048T>G) c.1798T>G (p.Ser600Ala) c.1402-10435T>G (n.1402-10435T>G) c.2134T>G (p.Ser712Ala) c.2314T>G (p.Ser772Ala) c.1981T>G (p.Ser661Ala) | |
7 | g.117592392C>A | CA368980489 | CFTR | c.2225C>A (p.Ser742Tyr) c.*1939C>A (n.*1939C>A) c.2042C>A (p.Ser681Tyr) c.*525C>A (n.*525C>A) c.*2049C>A (n.*2049C>A) c.1799C>A (p.Ser600Tyr) c.1402-10434C>A (n.1402-10434C>A) c.2135C>A (p.Ser712Tyr) c.2315C>A (p.Ser772Tyr) c.1982C>A (p.Ser661Tyr) | |
7 | g.117592392C= | CA1737395046 | CFTR | c.2225C= (p.Ser742=) c.*1939C= (n.*1939C=) c.2042C= (p.Ser681=) c.*525C= (n.*525C=) c.*2049C= (n.*2049C=) c.1799C= (p.Ser600=) c.1402-10434C= (n.1402-10434C=) c.2135C= (p.Ser712=) c.2315C= (p.Ser772=) c.1982C= (p.Ser661=) | |
7 | g.117592392C>G | CA368980491 | CFTR | c.2225C>G (p.Ser742Cys) c.*1939C>G (n.*1939C>G) c.2042C>G (p.Ser681Cys) c.*525C>G (n.*525C>G) c.*2049C>G (n.*2049C>G) c.1799C>G (p.Ser600Cys) c.1402-10434C>G (n.1402-10434C>G) c.2135C>G (p.Ser712Cys) c.2315C>G (p.Ser772Cys) c.1982C>G (p.Ser661Cys) | |
7 | g.117592392C>T | CA368980492 | CFTR | c.2225C>T (p.Ser742Phe) c.*1939C>T (n.*1939C>T) c.2042C>T (p.Ser681Phe) c.*525C>T (n.*525C>T) c.*2049C>T (n.*2049C>T) c.1799C>T (p.Ser600Phe) c.1402-10434C>T (n.1402-10434C>T) c.2135C>T (p.Ser712Phe) c.2315C>T (p.Ser772Phe) c.1982C>T (p.Ser661Phe) | ClinVar dbSNP gnomAD v4 |
7 | g.117592393T>A | CA457449485 | CFTR | c.2226T>A (p.Ser742=) c.*1940T>A (n.*1940T>A) c.2043T>A (p.Ser681=) c.*526T>A (n.*526T>A) c.*2050T>A (n.*2050T>A) c.1800T>A (p.Ser600=) c.1402-10433T>A (n.1402-10433T>A) c.2136T>A (p.Ser712=) c.2316T>A (p.Ser772=) c.1983T>A (p.Ser661=) | |
7 | g.117592393T>C | CA457449486 | CFTR | c.2226T>C (p.Ser742=) c.*1940T>C (n.*1940T>C) c.2043T>C (p.Ser681=) c.*526T>C (n.*526T>C) c.*2050T>C (n.*2050T>C) c.1800T>C (p.Ser600=) c.1402-10433T>C (n.1402-10433T>C) c.2136T>C (p.Ser712=) c.2316T>C (p.Ser772=) c.1983T>C (p.Ser661=) | ClinVar dbSNP gnomAD v4 |
7 | g.117592393T>G | CA457449487 | CFTR | c.2226T>G (p.Ser742=) c.*1940T>G (n.*1940T>G) c.2043T>G (p.Ser681=) c.*526T>G (n.*526T>G) c.*2050T>G (n.*2050T>G) c.1800T>G (p.Ser600=) c.1402-10433T>G (n.1402-10433T>G) c.2136T>G (p.Ser712=) c.2316T>G (p.Ser772=) c.1983T>G (p.Ser661=) | |
7 | g.117592394G>A | CA164948004 | CFTR | c.2227G>A (p.Glu743Lys) c.*1941G>A (n.*1941G>A) c.2044G>A (p.Glu682Lys) c.*527G>A (n.*527G>A) c.*2051G>A (n.*2051G>A) c.1801G>A (p.Glu601Lys) c.1402-10432G>A (n.1402-10432G>A) c.2137G>A (p.Glu713Lys) c.2317G>A (p.Glu773Lys) c.1984G>A (p.Glu662Lys) | dbSNP COSMIC |
7 | g.117592394G>C | CA368980494 | CFTR | c.2227G>C (p.Glu743Gln) c.*1941G>C (n.*1941G>C) c.2044G>C (p.Glu682Gln) c.*527G>C (n.*527G>C) c.*2051G>C (n.*2051G>C) c.1801G>C (p.Glu601Gln) c.1402-10432G>C (n.1402-10432G>C) c.2137G>C (p.Glu713Gln) c.2317G>C (p.Glu773Gln) c.1984G>C (p.Glu662Gln) | gnomAD v4 |
7 | g.117592394G= | CA1737395050 | CFTR | c.2227G= (p.Glu743=) c.*1941G= (n.*1941G=) c.2044G= (p.Glu682=) c.*527G= (n.*527G=) c.*2051G= (n.*2051G=) c.1801G= (p.Glu601=) c.1402-10432G= (n.1402-10432G=) c.2137G= (p.Glu713=) c.2317G= (p.Glu773=) c.1984G= (p.Glu662=) | |
7 | g.117592394G>T | CA368980496 | CFTR | c.2227G>T (p.Glu743Ter) c.*1941G>T (n.*1941G>T) c.2044G>T (p.Glu682Ter) c.*527G>T (n.*527G>T) c.*2051G>T (n.*2051G>T) c.1801G>T (p.Glu601Ter) c.1402-10432G>T (n.1402-10432G>T) c.2137G>T (p.Glu713Ter) c.2317G>T (p.Glu773Ter) c.1984G>T (p.Glu662Ter) | |
7 | g.117592395A>C | CA368980506 | CFTR | c.2228A>C (p.Glu743Ala) c.*1942A>C (n.*1942A>C) c.2045A>C (p.Glu682Ala) c.*528A>C (n.*528A>C) c.*2052A>C (n.*2052A>C) c.1802A>C (p.Glu601Ala) c.1402-10431A>C (n.1402-10431A>C) c.2138A>C (p.Glu713Ala) c.2318A>C (p.Glu773Ala) c.1985A>C (p.Glu662Ala) | |
7 | g.117592395A>G | CA368980501 | CFTR | c.2228A>G (p.Glu743Gly) c.*1942A>G (n.*1942A>G) c.2045A>G (p.Glu682Gly) c.*528A>G (n.*528A>G) c.*2052A>G (n.*2052A>G) c.1802A>G (p.Glu601Gly) c.1402-10431A>G (n.1402-10431A>G) c.2138A>G (p.Glu713Gly) c.2318A>G (p.Glu773Gly) c.1985A>G (p.Glu662Gly) | |
7 | g.117592395A>T | CA368980504 | CFTR | c.2228A>T (p.Glu743Val) c.*1942A>T (n.*1942A>T) c.2045A>T (p.Glu682Val) c.*528A>T (n.*528A>T) c.*2052A>T (n.*2052A>T) c.1802A>T (p.Glu601Val) c.1402-10431A>T (n.1402-10431A>T) c.2138A>T (p.Glu713Val) c.2318A>T (p.Glu773Val) c.1985A>T (p.Glu662Val) | |
7 | g.117592396G>A | CA457449491 | CFTR | c.2229G>A (p.Glu743=) c.*1943G>A (n.*1943G>A) c.2046G>A (p.Glu682=) c.*529G>A (n.*529G>A) c.*2053G>A (n.*2053G>A) c.1803G>A (p.Glu601=) c.1402-10430G>A (n.1402-10430G>A) c.2139G>A (p.Glu713=) c.2319G>A (p.Glu773=) c.1986G>A (p.Glu662=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
7 | g.117592396G>C | CA368980509 | CFTR | c.2229G>C (p.Glu743Asp) c.*1943G>C (n.*1943G>C) c.2046G>C (p.Glu682Asp) c.*529G>C (n.*529G>C) c.*2053G>C (n.*2053G>C) c.1803G>C (p.Glu601Asp) c.1402-10430G>C (n.1402-10430G>C) c.2139G>C (p.Glu713Asp) c.2319G>C (p.Glu773Asp) c.1986G>C (p.Glu662Asp) | |
7 | g.117592396G= | CA1737395053 | CFTR | c.2229G= (p.Glu743=) c.*1943G= (n.*1943G=) c.2046G= (p.Glu682=) c.*529G= (n.*529G=) c.*2053G= (n.*2053G=) c.1803G= (p.Glu601=) c.1402-10430G= (n.1402-10430G=) c.2139G= (p.Glu713=) c.2319G= (p.Glu773=) c.1986G= (p.Glu662=) | |
7 | g.117592396G>T | CA368980511 | CFTR | c.2229G>T (p.Glu743Asp) c.*1943G>T (n.*1943G>T) c.2046G>T (p.Glu682Asp) c.*529G>T (n.*529G>T) c.*2053G>T (n.*2053G>T) c.1803G>T (p.Glu601Asp) c.1402-10430G>T (n.1402-10430G>T) c.2139G>T (p.Glu713Asp) c.2319G>T (p.Glu773Asp) c.1986G>T (p.Glu662Asp) | |
7 | g.117592397C>A | CA368980514 | CFTR | c.2230C>A (p.Gln744Lys) c.*1944C>A (n.*1944C>A) c.2047C>A (p.Gln683Lys) c.*530C>A (n.*530C>A) c.*2054C>A (n.*2054C>A) c.1804C>A (p.Gln602Lys) c.1402-10429C>A (n.1402-10429C>A) c.2140C>A (p.Gln714Lys) c.2320C>A (p.Gln774Lys) c.1987C>A (p.Gln663Lys) | |
7 | g.117592397C>G | CA368980516 | CFTR | c.2230C>G (p.Gln744Glu) c.*1944C>G (n.*1944C>G) c.2047C>G (p.Gln683Glu) c.*530C>G (n.*530C>G) c.*2054C>G (n.*2054C>G) c.1804C>G (p.Gln602Glu) c.1402-10429C>G (n.1402-10429C>G) c.2140C>G (p.Gln714Glu) c.2320C>G (p.Gln774Glu) c.1987C>G (p.Gln663Glu) | |
7 | g.117592397C>T | CA368980518 | CFTR | c.2230C>T (p.Gln744Ter) c.*1944C>T (n.*1944C>T) c.2047C>T (p.Gln683Ter) c.*530C>T (n.*530C>T) c.*2054C>T (n.*2054C>T) c.1804C>T (p.Gln602Ter) c.1402-10429C>T (n.1402-10429C>T) c.2140C>T (p.Gln714Ter) c.2320C>T (p.Gln774Ter) c.1987C>T (p.Gln663Ter) | |
7 | g.117592398A= | CA1737395055 | CFTR | c.2231A= (p.Gln744=) c.*1945A= (n.*1945A=) c.2048A= (p.Gln683=) c.*531A= (n.*531A=) c.*2055A= (n.*2055A=) c.1805A= (p.Gln602=) c.1402-10428A= (n.1402-10428A=) c.2141A= (p.Gln714=) c.2321A= (p.Gln774=) c.1988A= (p.Gln663=) | |
7 | g.117592398A>C | CA368980519 | CFTR | c.2231A>C (p.Gln744Pro) c.*1945A>C (n.*1945A>C) c.2048A>C (p.Gln683Pro) c.*531A>C (n.*531A>C) c.*2055A>C (n.*2055A>C) c.1805A>C (p.Gln602Pro) c.1402-10428A>C (n.1402-10428A>C) c.2141A>C (p.Gln714Pro) c.2321A>C (p.Gln774Pro) c.1988A>C (p.Gln663Pro) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
7 | g.117592398A>G | CA368980520 | CFTR | c.2231A>G (p.Gln744Arg) c.*1945A>G (n.*1945A>G) c.2048A>G (p.Gln683Arg) c.*531A>G (n.*531A>G) c.*2055A>G (n.*2055A>G) c.1805A>G (p.Gln602Arg) c.1402-10428A>G (n.1402-10428A>G) c.2141A>G (p.Gln714Arg) c.2321A>G (p.Gln774Arg) c.1988A>G (p.Gln663Arg) | ClinVar gnomAD v4 |
7 | g.117592398A>T | CA368980522 | CFTR | c.2231A>T (p.Gln744Leu) c.*1945A>T (n.*1945A>T) c.2048A>T (p.Gln683Leu) c.*531A>T (n.*531A>T) c.*2055A>T (n.*2055A>T) c.1805A>T (p.Gln602Leu) c.1402-10428A>T (n.1402-10428A>T) c.2141A>T (p.Gln714Leu) c.2321A>T (p.Gln774Leu) c.1988A>T (p.Gln663Leu) | |
7 | g.117592399G>A | CA457449498 | CFTR | c.2232G>A (p.Gln744=) c.*1946G>A (n.*1946G>A) c.2049G>A (p.Gln683=) c.*532G>A (n.*532G>A) c.*2056G>A (n.*2056G>A) c.1806G>A (p.Gln602=) c.1402-10427G>A (n.1402-10427G>A) c.2142G>A (p.Gln714=) c.2322G>A (p.Gln774=) c.1989G>A (p.Gln663=) | |
7 | g.117592399G>C | CA368980525 | CFTR | c.2232G>C (p.Gln744His) c.*1946G>C (n.*1946G>C) c.2049G>C (p.Gln683His) c.*532G>C (n.*532G>C) c.*2056G>C (n.*2056G>C) c.1806G>C (p.Gln602His) c.1402-10427G>C (n.1402-10427G>C) c.2142G>C (p.Gln714His) c.2322G>C (p.Gln774His) c.1989G>C (p.Gln663His) | |
7 | g.117592399G>T | CA368980527 | CFTR | c.2232G>T (p.Gln744His) c.*1946G>T (n.*1946G>T) c.2049G>T (p.Gln683His) c.*532G>T (n.*532G>T) c.*2056G>T (n.*2056G>T) c.1806G>T (p.Gln602His) c.1402-10427G>T (n.1402-10427G>T) c.2142G>T (p.Gln714His) c.2322G>T (p.Gln774His) c.1989G>T (p.Gln663His) | |
7 | g.117592400G>A | CA368980530 | CFTR | c.2233G>A (p.Gly745Arg) c.*1947G>A (n.*1947G>A) c.2050G>A (p.Gly684Arg) c.*533G>A (n.*533G>A) c.*2057G>A (n.*2057G>A) c.1807G>A (p.Gly603Arg) c.1402-10426G>A (n.1402-10426G>A) c.2143G>A (p.Gly715Arg) c.2323G>A (p.Gly775Arg) c.1990G>A (p.Gly664Arg) | gnomAD v4 |
7 | g.117592400G>C | CA368980532 | CFTR | c.2233G>C (p.Gly745Arg) c.*1947G>C (n.*1947G>C) c.2050G>C (p.Gly684Arg) c.*533G>C (n.*533G>C) c.*2057G>C (n.*2057G>C) c.1807G>C (p.Gly603Arg) c.1402-10426G>C (n.1402-10426G>C) c.2143G>C (p.Gly715Arg) c.2323G>C (p.Gly775Arg) c.1990G>C (p.Gly664Arg) | |
7 | g.117592400G= | CA1737395058 | CFTR | c.2233G= (p.Gly745=) c.*1947G= (n.*1947G=) c.2050G= (p.Gly684=) c.*533G= (n.*533G=) c.*2057G= (n.*2057G=) c.1807G= (p.Gly603=) c.1402-10426G= (n.1402-10426G=) c.2143G= (p.Gly715=) c.2323G= (p.Gly775=) c.1990G= (p.Gly664=) | |
7 | g.117592400G>T | CA326772 | CFTR | c.2233G>T (p.Gly745Ter) c.*1947G>T (n.*1947G>T) c.2050G>T (p.Gly684Ter) c.*533G>T (n.*533G>T) c.*2057G>T (n.*2057G>T) c.1807G>T (p.Gly603Ter) c.1402-10426G>T (n.1402-10426G>T) c.2143G>T (p.Gly715Ter) c.2323G>T (p.Gly775Ter) c.1990G>T (p.Gly664Ter) | ClinVar dbSNP |
7 | g.117592401G>A | CA368980536 | CFTR | c.2234G>A (p.Gly745Glu) c.*1948G>A (n.*1948G>A) c.2051G>A (p.Gly684Glu) c.*534G>A (n.*534G>A) c.*2058G>A (n.*2058G>A) c.1808G>A (p.Gly603Glu) c.1402-10425G>A (n.1402-10425G>A) c.2144G>A (p.Gly715Glu) c.2324G>A (p.Gly775Glu) c.1991G>A (p.Gly664Glu) | gnomAD v4 |
7 | g.117592401G>C | CA368980540 | CFTR | c.2234G>C (p.Gly745Ala) c.*1948G>C (n.*1948G>C) c.2051G>C (p.Gly684Ala) c.*534G>C (n.*534G>C) c.*2058G>C (n.*2058G>C) c.1808G>C (p.Gly603Ala) c.1402-10425G>C (n.1402-10425G>C) c.2144G>C (p.Gly715Ala) c.2324G>C (p.Gly775Ala) c.1991G>C (p.Gly664Ala) | |
7 | g.117592401G>T | CA368980537 | CFTR | c.2234G>T (p.Gly745Val) c.*1948G>T (n.*1948G>T) c.2051G>T (p.Gly684Val) c.*534G>T (n.*534G>T) c.*2058G>T (n.*2058G>T) c.1808G>T (p.Gly603Val) c.1402-10425G>T (n.1402-10425G>T) c.2144G>T (p.Gly715Val) c.2324G>T (p.Gly775Val) c.1991G>T (p.Gly664Val) | |
7 | g.117592402A>C | CA457449503 | CFTR | c.2235A>C (p.Gly745=) c.*1949A>C (n.*1949A>C) c.2052A>C (p.Gly684=) c.*535A>C (n.*535A>C) c.*2059A>C (n.*2059A>C) c.1809A>C (p.Gly603=) c.1402-10424A>C (n.1402-10424A>C) c.2145A>C (p.Gly715=) c.2325A>C (p.Gly775=) c.1992A>C (p.Gly664=) | |
7 | g.117592402A>G | CA457449504 | CFTR | c.2235A>G (p.Gly745=) c.*1949A>G (n.*1949A>G) c.2052A>G (p.Gly684=) c.*535A>G (n.*535A>G) c.*2059A>G (n.*2059A>G) c.1809A>G (p.Gly603=) c.1402-10424A>G (n.1402-10424A>G) c.2145A>G (p.Gly715=) c.2325A>G (p.Gly775=) c.1992A>G (p.Gly664=) | ClinVar |
7 | g.117592402A>T | CA457449505 | CFTR | c.2235A>T (p.Gly745=) c.*1949A>T (n.*1949A>T) c.2052A>T (p.Gly684=) c.*535A>T (n.*535A>T) c.*2059A>T (n.*2059A>T) c.1809A>T (p.Gly603=) c.1402-10424A>T (n.1402-10424A>T) c.2145A>T (p.Gly715=) c.2325A>T (p.Gly775=) c.1992A>T (p.Gly664=) | |
7 | g.117592403G>A | CA368980542 | CFTR | c.2236G>A (p.Glu746Lys) c.*1950G>A (n.*1950G>A) c.2053G>A (p.Glu685Lys) c.*536G>A (n.*536G>A) c.*2060G>A (n.*2060G>A) c.1810G>A (p.Glu604Lys) c.1402-10423G>A (n.1402-10423G>A) c.2146G>A (p.Glu716Lys) c.2326G>A (p.Glu776Lys) c.1993G>A (p.Glu665Lys) | |
7 | g.117592403G>C | CA368980545 | CFTR | c.2236G>C (p.Glu746Gln) c.*1950G>C (n.*1950G>C) c.2053G>C (p.Glu685Gln) c.*536G>C (n.*536G>C) c.*2060G>C (n.*2060G>C) c.1810G>C (p.Glu604Gln) c.1402-10423G>C (n.1402-10423G>C) c.2146G>C (p.Glu716Gln) c.2326G>C (p.Glu776Gln) c.1993G>C (p.Glu665Gln) | |
7 | g.117592403G>T | CA368980547 | CFTR | c.2236G>T (p.Glu746Ter) c.*1950G>T (n.*1950G>T) c.2053G>T (p.Glu685Ter) c.*536G>T (n.*536G>T) c.*2060G>T (n.*2060G>T) c.1810G>T (p.Glu604Ter) c.1402-10423G>T (n.1402-10423G>T) c.2146G>T (p.Glu716Ter) c.2326G>T (p.Glu776Ter) c.1993G>T (p.Glu665Ter) | |
7 | g.117592403_117592413delinsAAAAATC | CA2695208514 | CFTR | c.2236_2246delinsAAAAATC (p.Glu746LysfsTer8) c.*1950_*1960delinsAAAAATC (n.*1950_*1960delinsAAAAATC) c.2053_2063delinsAAAAATC (p.Glu685LysfsTer8) c.*536_*546delinsAAAAATC (n.*536_*546delinsAAAAATC) c.*2060_*2070delinsAAAAATC (n.*2060_*2070delinsAAAAATC) c.1810_1820delinsAAAAATC (p.Glu604LysfsTer8) c.1402-10423_1402-10413delinsAAAAATC (n.1402-10423_1402-10413delinsAAAAATC) c.2146_2156delinsAAAAATC (p.Glu716LysfsTer8) c.2326_2336delinsAAAAATC (p.Glu776LysfsTer8) c.1993_2003delinsAAAAATC (p.Glu665LysfsTer8) | |
7 | g.117592404_117592414del | CA2695208515 | CFTR | c.2237_2247del (p.Glu746AlafsTer29) c.*1951_*1961del (n.*1951_*1961del) c.2054_2064del (p.Glu685AlafsTer29) c.*537_*547del (n.*537_*547del) c.*2061_*2071del (n.*2061_*2071del) c.1811_1821del (p.Glu604AlafsTer29) c.1402-10422_1402-10412del (n.1402-10422_1402-10412del) c.2147_2157del (p.Glu716AlafsTer29) c.2327_2337del (p.Glu776AlafsTer29) c.1994_2004del (p.Glu665AlafsTer29) | |
7 | g.117592404A>C | CA368980550 | CFTR | c.2237A>C (p.Glu746Ala) c.*1951A>C (n.*1951A>C) c.2054A>C (p.Glu685Ala) c.*537A>C (n.*537A>C) c.*2061A>C (n.*2061A>C) c.1811A>C (p.Glu604Ala) c.1402-10422A>C (n.1402-10422A>C) c.2147A>C (p.Glu716Ala) c.2327A>C (p.Glu776Ala) c.1994A>C (p.Glu665Ala) | |
7 | g.117592404A>G | CA368980552 | CFTR | c.2237A>G (p.Glu746Gly) c.*1951A>G (n.*1951A>G) c.2054A>G (p.Glu685Gly) c.*537A>G (n.*537A>G) c.*2061A>G (n.*2061A>G) c.1811A>G (p.Glu604Gly) c.1402-10422A>G (n.1402-10422A>G) c.2147A>G (p.Glu716Gly) c.2327A>G (p.Glu776Gly) c.1994A>G (p.Glu665Gly) | |
7 | g.117592404A>T | CA368980554 | CFTR | c.2237A>T (p.Glu746Val) c.*1951A>T (n.*1951A>T) c.2054A>T (p.Glu685Val) c.*537A>T (n.*537A>T) c.*2061A>T (n.*2061A>T) c.1811A>T (p.Glu604Val) c.1402-10422A>T (n.1402-10422A>T) c.2147A>T (p.Glu716Val) c.2327A>T (p.Glu776Val) c.1994A>T (p.Glu665Val) | |
7 | g.117592405G>A | CA457449509 | CFTR | c.2238G>A (p.Glu746=) c.*1952G>A (n.*1952G>A) c.2055G>A (p.Glu685=) c.*538G>A (n.*538G>A) c.*2062G>A (n.*2062G>A) c.1812G>A (p.Glu604=) c.1402-10421G>A (n.1402-10421G>A) c.2148G>A (p.Glu716=) c.2328G>A (p.Glu776=) c.1995G>A (p.Glu665=) | dbSNP |
7 | g.117592405G>C | CA368980557 | CFTR | c.2238G>C (p.Glu746Asp) c.*1952G>C (n.*1952G>C) c.2055G>C (p.Glu685Asp) c.*538G>C (n.*538G>C) c.*2062G>C (n.*2062G>C) c.1812G>C (p.Glu604Asp) c.1402-10421G>C (n.1402-10421G>C) c.2148G>C (p.Glu716Asp) c.2328G>C (p.Glu776Asp) c.1995G>C (p.Glu665Asp) | ClinVar |
7 | g.117592405G= | CA1737395065 | CFTR | c.2238G= (p.Glu746=) c.*1952G= (n.*1952G=) c.2055G= (p.Glu685=) c.*538G= (n.*538G=) c.*2062G= (n.*2062G=) c.1812G= (p.Glu604=) c.1402-10421G= (n.1402-10421G=) c.2148G= (p.Glu716=) c.2328G= (p.Glu776=) c.1995G= (p.Glu665=) | |
7 | g.117592405G>T | CA368980559 | CFTR | c.2238G>T (p.Glu746Asp) c.*1952G>T (n.*1952G>T) c.2055G>T (p.Glu685Asp) c.*538G>T (n.*538G>T) c.*2062G>T (n.*2062G>T) c.1812G>T (p.Glu604Asp) c.1402-10421G>T (n.1402-10421G>T) c.2148G>T (p.Glu716Asp) c.2328G>T (p.Glu776Asp) c.1995G>T (p.Glu665Asp) | |
7 | g.117592405_117592413delinsGGCGATACT | CA1737395063 | CFTR | c.2238_2246delinsGGCGATACT (p.Glu746=) c.*1952_*1960delinsGGCGATACT (n.*1952_*1960delinsGGCGATACT) c.2055_2063delinsGGCGATACT (p.Glu685=) c.*538_*546delinsGGCGATACT (n.*538_*546delinsGGCGATACT) c.*2062_*2070delinsGGCGATACT (n.*2062_*2070delinsGGCGATACT) c.1812_1820delinsGGCGATACT (p.Glu604=) c.1402-10421_1402-10413delinsGGCGATACT (n.1402-10421_1402-10413delinsGGCGATACT) c.2148_2156delinsGGCGATACT (p.Glu716=) c.2328_2336delinsGGCGATACT (p.Glu776=) c.1995_2003delinsGGCGATACT (p.Glu665=) | |
7 | g.117592406G>A | CA368980563 | CFTR | c.2239G>A (p.Ala747Thr) c.*1953G>A (n.*1953G>A) c.2056G>A (p.Ala686Thr) c.*539G>A (n.*539G>A) c.*2063G>A (n.*2063G>A) c.1813G>A (p.Ala605Thr) c.1402-10420G>A (n.1402-10420G>A) c.2149G>A (p.Ala717Thr) c.2329G>A (p.Ala777Thr) c.1996G>A (p.Ala666Thr) | gnomAD v4 |
7 | g.117592406G>C | CA368980565 | CFTR | c.2239G>C (p.Ala747Pro) c.*1953G>C (n.*1953G>C) c.2056G>C (p.Ala686Pro) c.*539G>C (n.*539G>C) c.*2063G>C (n.*2063G>C) c.1813G>C (p.Ala605Pro) c.1402-10420G>C (n.1402-10420G>C) c.2149G>C (p.Ala717Pro) c.2329G>C (p.Ala777Pro) c.1996G>C (p.Ala666Pro) | |
7 | g.117592406G>T | CA368980568 | CFTR | c.2239G>T (p.Ala747Ser) c.*1953G>T (n.*1953G>T) c.2056G>T (p.Ala686Ser) c.*539G>T (n.*539G>T) c.*2063G>T (n.*2063G>T) c.1813G>T (p.Ala605Ser) c.1402-10420G>T (n.1402-10420G>T) c.2149G>T (p.Ala717Ser) c.2329G>T (p.Ala777Ser) c.1996G>T (p.Ala666Ser) | |
7 | g.117592408_117592415del | CA326774 | CFTR | c.2241_2248del (p.Ile748SerfsTer28) c.*1955_*1962del (n.*1955_*1962del) c.2058_2065del (p.Ile687SerfsTer28) c.*541_*548del (n.*541_*548del) c.*2065_*2072del (n.*2065_*2072del) c.1815_1822del (p.Ile606SerfsTer28) c.1402-10418_1402-10411del (n.1402-10418_1402-10411del) c.2151_2158del (p.Ile718SerfsTer28) c.2331_2338del (p.Ile778SerfsTer28) c.1998_2005del (p.Ile667SerfsTer28) | ClinVar dbSNP |
7 | g.117592407C>A | CA368980576 | CFTR | c.2240C>A (p.Ala747Glu) c.*1954C>A (n.*1954C>A) c.2057C>A (p.Ala686Glu) c.*540C>A (n.*540C>A) c.*2064C>A (n.*2064C>A) c.1814C>A (p.Ala605Glu) c.1402-10419C>A (n.1402-10419C>A) c.2150C>A (p.Ala717Glu) c.2330C>A (p.Ala777Glu) c.1997C>A (p.Ala666Glu) | ClinVar |
7 | g.117592407C= | CA1737395072 | CFTR | c.2240C= (p.Ala747=) c.*1954C= (n.*1954C=) c.2057C= (p.Ala686=) c.*540C= (n.*540C=) c.*2064C= (n.*2064C=) c.1814C= (p.Ala605=) c.1402-10419C= (n.1402-10419C=) c.2150C= (p.Ala717=) c.2330C= (p.Ala777=) c.1997C= (p.Ala666=) | |
7 | g.117592407C>G | CA368980574 | CFTR | c.2240C>G (p.Ala747Gly) c.*1954C>G (n.*1954C>G) c.2057C>G (p.Ala686Gly) c.*540C>G (n.*540C>G) c.*2064C>G (n.*2064C>G) c.1814C>G (p.Ala605Gly) c.1402-10419C>G (n.1402-10419C>G) c.2150C>G (p.Ala717Gly) c.2330C>G (p.Ala777Gly) c.1997C>G (p.Ala666Gly) | |
7 | g.117592407C>T | CA4451156 | CFTR | c.2240C>T (p.Ala747Val) c.*1954C>T (n.*1954C>T) c.2057C>T (p.Ala686Val) c.*540C>T (n.*540C>T) c.*2064C>T (n.*2064C>T) c.1814C>T (p.Ala605Val) c.1402-10419C>T (n.1402-10419C>T) c.2150C>T (p.Ala717Val) c.2330C>T (p.Ala777Val) c.1997C>T (p.Ala666Val) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.117592408del | CA2580076537 | CFTR | c.2241del (p.Ile748TyrfsTer7) c.*1955del (n.*1955del) c.2058del (p.Ile687TyrfsTer7) c.*541del (n.*541del) c.*2065del (n.*2065del) c.1815del (p.Ile606TyrfsTer7) c.1402-10418del (n.1402-10418del) c.2151del (p.Ile718TyrfsTer7) c.2331del (p.Ile778TyrfsTer7) c.1998del (p.Ile667TyrfsTer7) | ClinVar |
7 | g.117592408G>A | CA4451157 | CFTR | c.2241G>A (p.Ala747=) c.*1955G>A (n.*1955G>A) c.2058G>A (p.Ala686=) c.*541G>A (n.*541G>A) c.*2065G>A (n.*2065G>A) c.1815G>A (p.Ala605=) c.1402-10418G>A (n.1402-10418G>A) c.2151G>A (p.Ala717=) c.2331G>A (p.Ala777=) c.1998G>A (p.Ala666=) | ClinVar dbSNP ExAC gnomAD v3 gnomAD v4 |
7 | g.117592408G>C | CA457449521 | CFTR | c.2241G>C (p.Ala747=) c.*1955G>C (n.*1955G>C) c.2058G>C (p.Ala686=) c.*541G>C (n.*541G>C) c.*2065G>C (n.*2065G>C) c.1815G>C (p.Ala605=) c.1402-10418G>C (n.1402-10418G>C) c.2151G>C (p.Ala717=) c.2331G>C (p.Ala777=) c.1998G>C (p.Ala666=) | |
7 | g.117592408G= | CA1737395075 | CFTR | c.2241G= (p.Ala747=) c.*1955G= (n.*1955G=) c.2058G= (p.Ala686=) c.*541G= (n.*541G=) c.*2065G= (n.*2065G=) c.1815G= (p.Ala605=) c.1402-10418G= (n.1402-10418G=) c.2151G= (p.Ala717=) c.2331G= (p.Ala777=) c.1998G= (p.Ala666=) | |
7 | g.117592408G>T | CA457449522 | CFTR | c.2241G>T (p.Ala747=) c.*1955G>T (n.*1955G>T) c.2058G>T (p.Ala686=) c.*541G>T (n.*541G>T) c.*2065G>T (n.*2065G>T) c.1815G>T (p.Ala605=) c.1402-10418G>T (n.1402-10418G>T) c.2151G>T (p.Ala717=) c.2331G>T (p.Ala777=) c.1998G>T (p.Ala666=) | |
7 | g.117592409A>C | CA368980586 | CFTR | c.2242A>C (p.Ile748Leu) c.*1956A>C (n.*1956A>C) c.2059A>C (p.Ile687Leu) c.*542A>C (n.*542A>C) c.*2066A>C (n.*2066A>C) c.1816A>C (p.Ile606Leu) c.1402-10417A>C (n.1402-10417A>C) c.2152A>C (p.Ile718Leu) c.2332A>C (p.Ile778Leu) c.1999A>C (p.Ile667Leu) | |
7 | g.117592409A>G | CA368980588 | CFTR | c.2242A>G (p.Ile748Val) c.*1956A>G (n.*1956A>G) c.2059A>G (p.Ile687Val) c.*542A>G (n.*542A>G) c.*2066A>G (n.*2066A>G) c.1816A>G (p.Ile606Val) c.1402-10417A>G (n.1402-10417A>G) c.2152A>G (p.Ile718Val) c.2332A>G (p.Ile778Val) c.1999A>G (p.Ile667Val) | |
7 | g.117592409A>T | CA368980590 | CFTR | c.2242A>T (p.Ile748Leu) c.*1956A>T (n.*1956A>T) c.2059A>T (p.Ile687Leu) c.*542A>T (n.*542A>T) c.*2066A>T (n.*2066A>T) c.1816A>T (p.Ile606Leu) c.1402-10417A>T (n.1402-10417A>T) c.2152A>T (p.Ile718Leu) c.2332A>T (p.Ile778Leu) c.1999A>T (p.Ile667Leu) | |
7 | g.117592410T>A | CA368980593 | CFTR | c.2243T>A (p.Ile748Lys) c.*1957T>A (n.*1957T>A) c.2060T>A (p.Ile687Lys) c.*543T>A (n.*543T>A) c.*2067T>A (n.*2067T>A) c.1817T>A (p.Ile606Lys) c.1402-10416T>A (n.1402-10416T>A) c.2153T>A (p.Ile718Lys) c.2333T>A (p.Ile778Lys) c.2000T>A (p.Ile667Lys) | |
7 | g.117592410T>C | CA368980595 | CFTR | c.2243T>C (p.Ile748Thr) c.*1957T>C (n.*1957T>C) c.2060T>C (p.Ile687Thr) c.*543T>C (n.*543T>C) c.*2067T>C (n.*2067T>C) c.1817T>C (p.Ile606Thr) c.1402-10416T>C (n.1402-10416T>C) c.2153T>C (p.Ile718Thr) c.2333T>C (p.Ile778Thr) c.2000T>C (p.Ile667Thr) | gnomAD v4 COSMIC |
7 | g.117592410T>G | CA368980598 | CFTR | c.2243T>G (p.Ile748Arg) c.*1957T>G (n.*1957T>G) c.2060T>G (p.Ile687Arg) c.*543T>G (n.*543T>G) c.*2067T>G (n.*2067T>G) c.1817T>G (p.Ile606Arg) c.1402-10416T>G (n.1402-10416T>G) c.2153T>G (p.Ile718Arg) c.2333T>G (p.Ile778Arg) c.2000T>G (p.Ile667Arg) | |
7 | g.117592411A>C | CA457449530 | CFTR | c.2244A>C (p.Ile748=) c.*1958A>C (n.*1958A>C) c.2061A>C (p.Ile687=) c.*544A>C (n.*544A>C) c.*2068A>C (n.*2068A>C) c.1818A>C (p.Ile606=) c.1402-10415A>C (n.1402-10415A>C) c.2154A>C (p.Ile718=) c.2334A>C (p.Ile778=) c.2001A>C (p.Ile667=) | |
7 | g.117592411A>G | CA368980600 | CFTR | c.2244A>G (p.Ile748Met) c.*1958A>G (n.*1958A>G) c.2061A>G (p.Ile687Met) c.*544A>G (n.*544A>G) c.*2068A>G (n.*2068A>G) c.1818A>G (p.Ile606Met) c.1402-10415A>G (n.1402-10415A>G) c.2154A>G (p.Ile718Met) c.2334A>G (p.Ile778Met) c.2001A>G (p.Ile667Met) | |
7 | g.117592411A>T | CA457449531 | CFTR | c.2244A>T (p.Ile748=) c.*1958A>T (n.*1958A>T) c.2061A>T (p.Ile687=) c.*544A>T (n.*544A>T) c.*2068A>T (n.*2068A>T) c.1818A>T (p.Ile606=) c.1402-10415A>T (n.1402-10415A>T) c.2154A>T (p.Ile718=) c.2334A>T (p.Ile778=) c.2001A>T (p.Ile667=) | |
7 | g.117592412C>A | CA368980604 | CFTR | c.2245C>A (p.Leu749Met) c.*1959C>A (n.*1959C>A) c.2062C>A (p.Leu688Met) c.*545C>A (n.*545C>A) c.*2069C>A (n.*2069C>A) c.1819C>A (p.Leu607Met) c.1402-10414C>A (n.1402-10414C>A) c.2155C>A (p.Leu719Met) c.2335C>A (p.Leu779Met) c.2002C>A (p.Leu668Met) | dbSNP |
7 | g.117592412C= | CA1737395080 | CFTR | c.2245C= (p.Leu749=) c.*1959C= (n.*1959C=) c.2062C= (p.Leu688=) c.*545C= (n.*545C=) c.*2069C= (n.*2069C=) c.1819C= (p.Leu607=) c.1402-10414C= (n.1402-10414C=) c.2155C= (p.Leu719=) c.2335C= (p.Leu779=) c.2002C= (p.Leu668=) | |
7 | g.117592412C>G | CA368980607 | CFTR | c.2245C>G (p.Leu749Val) c.*1959C>G (n.*1959C>G) c.2062C>G (p.Leu688Val) c.*545C>G (n.*545C>G) c.*2069C>G (n.*2069C>G) c.1819C>G (p.Leu607Val) c.1402-10414C>G (n.1402-10414C>G) c.2155C>G (p.Leu719Val) c.2335C>G (p.Leu779Val) c.2002C>G (p.Leu668Val) | |
7 | g.117592412C>T | CA4451158 | CFTR | c.2245C>T (p.Leu749=) c.*1959C>T (n.*1959C>T) c.2062C>T (p.Leu688=) c.*545C>T (n.*545C>T) c.*2069C>T (n.*2069C>T) c.1819C>T (p.Leu607=) c.1402-10414C>T (n.1402-10414C>T) c.2155C>T (p.Leu719=) c.2335C>T (p.Leu779=) c.2002C>T (p.Leu668=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.117592413_117592415del | CA2684619360 | CFTR | c.2246_2248del (p.Leu749del) c.*1960_*1962del (n.*1960_*1962del) c.2063_2065del (p.Leu688del) c.*546_*548del (n.*546_*548del) c.*2070_*2072del (n.*2070_*2072del) c.1820_1822del (p.Leu607del) c.1402-10413_1402-10411del (n.1402-10413_1402-10411del) c.2156_2158del (p.Leu719del) c.2336_2338del (p.Leu779del) c.2003_2005del (p.Leu668del) | gnomAD v4 |
7 | g.117592413T>A | CA368980619 | CFTR | c.2246T>A (p.Leu749Gln) c.*1960T>A (n.*1960T>A) c.2063T>A (p.Leu688Gln) c.*546T>A (n.*546T>A) c.*2070T>A (n.*2070T>A) c.1820T>A (p.Leu607Gln) c.1402-10413T>A (n.1402-10413T>A) c.2156T>A (p.Leu719Gln) c.2336T>A (p.Leu779Gln) c.2003T>A (p.Leu668Gln) | gnomAD v4 |
7 | g.117592413T>C | CA368980616 | CFTR | c.2246T>C (p.Leu749Pro) c.*1960T>C (n.*1960T>C) c.2063T>C (p.Leu688Pro) c.*546T>C (n.*546T>C) c.*2070T>C (n.*2070T>C) c.1820T>C (p.Leu607Pro) c.1402-10413T>C (n.1402-10413T>C) c.2156T>C (p.Leu719Pro) c.2336T>C (p.Leu779Pro) c.2003T>C (p.Leu668Pro) | |
7 | g.117592413T>G | CA368980614 | CFTR | c.2246T>G (p.Leu749Arg) c.*1960T>G (n.*1960T>G) c.2063T>G (p.Leu688Arg) c.*546T>G (n.*546T>G) c.*2070T>G (n.*2070T>G) c.1820T>G (p.Leu607Arg) c.1402-10413T>G (n.1402-10413T>G) c.2156T>G (p.Leu719Arg) c.2336T>G (p.Leu779Arg) c.2003T>G (p.Leu668Arg) | |
7 | g.117592414G>A | CA457449544 | CFTR | c.2247G>A (p.Leu749=) c.*1961G>A (n.*1961G>A) c.2064G>A (p.Leu688=) c.*547G>A (n.*547G>A) c.*2071G>A (n.*2071G>A) c.1821G>A (p.Leu607=) c.1402-10412G>A (n.1402-10412G>A) c.2157G>A (p.Leu719=) c.2337G>A (p.Leu779=) c.2004G>A (p.Leu668=) | |
7 | g.117592414G>C | CA457449546 | CFTR | c.2247G>C (p.Leu749=) c.*1961G>C (n.*1961G>C) c.2064G>C (p.Leu688=) c.*547G>C (n.*547G>C) c.*2071G>C (n.*2071G>C) c.1821G>C (p.Leu607=) c.1402-10412G>C (n.1402-10412G>C) c.2157G>C (p.Leu719=) c.2337G>C (p.Leu779=) c.2004G>C (p.Leu668=) | dbSNP |
7 | g.117592414G= | CA1737395085 | CFTR | c.2247G= (p.Leu749=) c.*1961G= (n.*1961G=) c.2064G= (p.Leu688=) c.*547G= (n.*547G=) c.*2071G= (n.*2071G=) c.1821G= (p.Leu607=) c.1402-10412G= (n.1402-10412G=) c.2157G= (p.Leu719=) c.2337G= (p.Leu779=) c.2004G= (p.Leu668=) | |
7 | g.117592414G>T | CA457449548 | CFTR | c.2247G>T (p.Leu749=) c.*1961G>T (n.*1961G>T) c.2064G>T (p.Leu688=) c.*547G>T (n.*547G>T) c.*2071G>T (n.*2071G>T) c.1821G>T (p.Leu607=) c.1402-10412G>T (n.1402-10412G>T) c.2157G>T (p.Leu719=) c.2337G>T (p.Leu779=) c.2004G>T (p.Leu668=) | |
7 | g.117592414_117592422delinsGCCTCGCAT | CA1737395083 | CFTR | c.2247_2255delinsGCCTCGCAT (p.Leu749=) c.*1961_*1969delinsGCCTCGCAT (n.*1961_*1969delinsGCCTCGCAT) c.2064_2072delinsGCCTCGCAT (p.Leu688=) c.*547_*555delinsGCCTCGCAT (n.*547_*555delinsGCCTCGCAT) c.*2071_*2079delinsGCCTCGCAT (n.*2071_*2079delinsGCCTCGCAT) c.1821_1829delinsGCCTCGCAT (p.Leu607=) c.1402-10412_1402-10404delinsGCCTCGCAT (n.1402-10412_1402-10404delinsGCCTCGCAT) c.2157_2165delinsGCCTCGCAT (p.Leu719=) c.2337_2345delinsGCCTCGCAT (p.Leu779=) c.2004_2012delinsGCCTCGCAT (p.Leu668=) | |
7 | g.117592415C>A | CA368980622 | CFTR | c.2248C>A (p.Pro750Thr) c.*1962C>A (n.*1962C>A) c.2065C>A (p.Pro689Thr) c.*548C>A (n.*548C>A) c.*2072C>A (n.*2072C>A) c.1822C>A (p.Pro608Thr) c.1402-10411C>A (n.1402-10411C>A) c.2158C>A (p.Pro720Thr) c.2338C>A (p.Pro780Thr) c.2005C>A (p.Pro669Thr) | ClinVar |
7 | g.117592415C>G | CA368980624 | CFTR | c.2248C>G (p.Pro750Ala) c.*1962C>G (n.*1962C>G) c.2065C>G (p.Pro689Ala) c.*548C>G (n.*548C>G) c.*2072C>G (n.*2072C>G) c.1822C>G (p.Pro608Ala) c.1402-10411C>G (n.1402-10411C>G) c.2158C>G (p.Pro720Ala) c.2338C>G (p.Pro780Ala) c.2005C>G (p.Pro669Ala) | |
7 | g.117592415C>T | CA368980626 | CFTR | c.2248C>T (p.Pro750Ser) c.*1962C>T (n.*1962C>T) c.2065C>T (p.Pro689Ser) c.*548C>T (n.*548C>T) c.*2072C>T (n.*2072C>T) c.1822C>T (p.Pro608Ser) c.1402-10411C>T (n.1402-10411C>T) c.2158C>T (p.Pro720Ser) c.2338C>T (p.Pro780Ser) c.2005C>T (p.Pro669Ser) | |
7 | g.117592416_117592423del | CA326775 | CFTR | c.2249_2256del (p.Pro750GlnfsTer26) c.*1963_*1970del (n.*1963_*1970del) c.2066_2073del (p.Pro689GlnfsTer26) c.*549_*556del (n.*549_*556del) c.*2073_*2080del (n.*2073_*2080del) c.1823_1830del (p.Pro608GlnfsTer26) c.1402-10410_1402-10403del (n.1402-10410_1402-10403del) c.2159_2166del (p.Pro720GlnfsTer26) c.2339_2346del (p.Pro780GlnfsTer26) c.2006_2013del (p.Pro669GlnfsTer26) | ClinVar dbSNP |
7 | g.117592416C>A | CA368980630 | CFTR | c.2249C>A (p.Pro750His) c.*1963C>A (n.*1963C>A) c.2066C>A (p.Pro689His) c.*549C>A (n.*549C>A) c.*2073C>A (n.*2073C>A) c.1823C>A (p.Pro608His) c.1402-10410C>A (n.1402-10410C>A) c.2159C>A (p.Pro720His) c.2339C>A (p.Pro780His) c.2006C>A (p.Pro669His) | |
7 | g.117592416C= | CA1737395094 | CFTR | c.2249C= (p.Pro750=) c.*1963C= (n.*1963C=) c.2066C= (p.Pro689=) c.*549C= (n.*549C=) c.*2073C= (n.*2073C=) c.1823C= (p.Pro608=) c.1402-10410C= (n.1402-10410C=) c.2159C= (p.Pro720=) c.2339C= (p.Pro780=) c.2006C= (p.Pro669=) | |
7 | g.117592416C>G | CA368980632 | CFTR | c.2249C>G (p.Pro750Arg) c.*1963C>G (n.*1963C>G) c.2066C>G (p.Pro689Arg) c.*549C>G (n.*549C>G) c.*2073C>G (n.*2073C>G) c.1823C>G (p.Pro608Arg) c.1402-10410C>G (n.1402-10410C>G) c.2159C>G (p.Pro720Arg) c.2339C>G (p.Pro780Arg) c.2006C>G (p.Pro669Arg) | |
7 | g.117592416C>T | CA221011 | CFTR | c.2249C>T (p.Pro750Leu) c.*1963C>T (n.*1963C>T) c.2066C>T (p.Pro689Leu) c.*549C>T (n.*549C>T) c.*2073C>T (n.*2073C>T) c.1823C>T (p.Pro608Leu) c.1402-10410C>T (n.1402-10410C>T) c.2159C>T (p.Pro720Leu) c.2339C>T (p.Pro780Leu) c.2006C>T (p.Pro669Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.117592417T>A | CA457449554 | CFTR | c.2250T>A (p.Pro750=) c.*1964T>A (n.*1964T>A) c.2067T>A (p.Pro689=) c.*550T>A (n.*550T>A) c.*2074T>A (n.*2074T>A) c.1824T>A (p.Pro608=) c.1402-10409T>A (n.1402-10409T>A) c.2160T>A (p.Pro720=) c.2340T>A (p.Pro780=) c.2007T>A (p.Pro669=) | |
7 | g.117592417T>C | CA457449555 | CFTR | c.2250T>C (p.Pro750=) c.*1964T>C (n.*1964T>C) c.2067T>C (p.Pro689=) c.*550T>C (n.*550T>C) c.*2074T>C (n.*2074T>C) c.1824T>C (p.Pro608=) c.1402-10409T>C (n.1402-10409T>C) c.2160T>C (p.Pro720=) c.2340T>C (p.Pro780=) c.2007T>C (p.Pro669=) | |
7 | g.117592417T>G | CA457449556 | CFTR | c.2250T>G (p.Pro750=) c.*1964T>G (n.*1964T>G) c.2067T>G (p.Pro689=) c.*550T>G (n.*550T>G) c.*2074T>G (n.*2074T>G) c.1824T>G (p.Pro608=) c.1402-10409T>G (n.1402-10409T>G) c.2160T>G (p.Pro720=) c.2340T>G (p.Pro780=) c.2007T>G (p.Pro669=) | |
7 | g.117592418C>A | CA368980639 | CFTR | c.2251C>A (p.Arg751Ser) c.*1965C>A (n.*1965C>A) c.2068C>A (p.Arg690Ser) c.*551C>A (n.*551C>A) c.*2075C>A (n.*2075C>A) c.1825C>A (p.Arg609Ser) c.1402-10408C>A (n.1402-10408C>A) c.2161C>A (p.Arg721Ser) c.2341C>A (p.Arg781Ser) c.2008C>A (p.Arg670Ser) | |
7 | g.117592418C= | CA1737395098 | CFTR | c.2251C= (p.Arg751=) c.*1965C= (n.*1965C=) c.2068C= (p.Arg690=) c.*551C= (n.*551C=) c.*2075C= (n.*2075C=) c.1825C= (p.Arg609=) c.1402-10408C= (n.1402-10408C=) c.2161C= (p.Arg721=) c.2341C= (p.Arg781=) c.2008C= (p.Arg670=) | |
7 | g.117592418C>G | CA368980643 | CFTR | c.2251C>G (p.Arg751Gly) c.*1965C>G (n.*1965C>G) c.2068C>G (p.Arg690Gly) c.*551C>G (n.*551C>G) c.*2075C>G (n.*2075C>G) c.1825C>G (p.Arg609Gly) c.1402-10408C>G (n.1402-10408C>G) c.2161C>G (p.Arg721Gly) c.2341C>G (p.Arg781Gly) c.2008C>G (p.Arg670Gly) | gnomAD v4 |
7 | g.117592418C>T | CA4451159 | CFTR | c.2251C>T (p.Arg751Cys) c.*1965C>T (n.*1965C>T) c.2068C>T (p.Arg690Cys) c.*551C>T (n.*551C>T) c.*2075C>T (n.*2075C>T) c.1825C>T (p.Arg609Cys) c.1402-10408C>T (n.1402-10408C>T) c.2161C>T (p.Arg721Cys) c.2341C>T (p.Arg781Cys) c.2008C>T (p.Arg670Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.117592419G>A | CA4451160 | CFTR | c.2252G>A (p.Arg751His) c.*1966G>A (n.*1966G>A) c.2069G>A (p.Arg690His) c.*552G>A (n.*552G>A) c.*2076G>A (n.*2076G>A) c.1826G>A (p.Arg609His) c.1402-10407G>A (n.1402-10407G>A) c.2162G>A (p.Arg721His) c.2342G>A (p.Arg781His) c.2009G>A (p.Arg670His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.117592419G>C | CA326778 | CFTR | c.2252G>C (p.Arg751Pro) c.*1966G>C (n.*1966G>C) c.2069G>C (p.Arg690Pro) c.*552G>C (n.*552G>C) c.*2076G>C (n.*2076G>C) c.1826G>C (p.Arg609Pro) c.1402-10407G>C (n.1402-10407G>C) c.2162G>C (p.Arg721Pro) c.2342G>C (p.Arg781Pro) c.2009G>C (p.Arg670Pro) | dbSNP |
7 | g.117592419G= | CA1737395104 | CFTR | c.2252G= (p.Arg751=) c.*1966G= (n.*1966G=) c.2069G= (p.Arg690=) c.*552G= (n.*552G=) c.*2076G= (n.*2076G=) c.1826G= (p.Arg609=) c.1402-10407G= (n.1402-10407G=) c.2162G= (p.Arg721=) c.2342G= (p.Arg781=) c.2009G= (p.Arg670=) | |
7 | g.117592419G>T | CA10581251 | CFTR | c.2252G>T (p.Arg751Leu) c.*1966G>T (n.*1966G>T) c.2069G>T (p.Arg690Leu) c.*552G>T (n.*552G>T) c.*2076G>T (n.*2076G>T) c.1826G>T (p.Arg609Leu) c.1402-10407G>T (n.1402-10407G>T) c.2162G>T (p.Arg721Leu) c.2342G>T (p.Arg781Leu) c.2009G>T (p.Arg670Leu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
7 | g.117592420C>A | CA457449558 | CFTR | c.2253C>A (p.Arg751=) c.*1967C>A (n.*1967C>A) c.2070C>A (p.Arg690=) c.*553C>A (n.*553C>A) c.*2077C>A (n.*2077C>A) c.1827C>A (p.Arg609=) c.1402-10406C>A (n.1402-10406C>A) c.2163C>A (p.Arg721=) c.2343C>A (p.Arg781=) c.2010C>A (p.Arg670=) | |
7 | g.117592420C= | CA1737395110 | CFTR | c.2253C= (p.Arg751=) c.*1967C= (n.*1967C=) c.2070C= (p.Arg690=) c.*553C= (n.*553C=) c.*2077C= (n.*2077C=) c.1827C= (p.Arg609=) c.1402-10406C= (n.1402-10406C=) c.2163C= (p.Arg721=) c.2343C= (p.Arg781=) c.2010C= (p.Arg670=) | |
7 | g.117592420C>G | CA457449559 | CFTR | c.2253C>G (p.Arg751=) c.*1967C>G (n.*1967C>G) c.2070C>G (p.Arg690=) c.*553C>G (n.*553C>G) c.*2077C>G (n.*2077C>G) c.1827C>G (p.Arg609=) c.1402-10406C>G (n.1402-10406C>G) c.2163C>G (p.Arg721=) c.2343C>G (p.Arg781=) c.2010C>G (p.Arg670=) | |
7 | g.117592420C>T | CA4451161 | CFTR | c.2253C>T (p.Arg751=) c.*1967C>T (n.*1967C>T) c.2070C>T (p.Arg690=) c.*553C>T (n.*553C>T) c.*2077C>T (n.*2077C>T) c.1827C>T (p.Arg609=) c.1402-10406C>T (n.1402-10406C>T) c.2163C>T (p.Arg721=) c.2343C>T (p.Arg781=) c.2010C>T (p.Arg670=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.117592421A>C | CA368980659 | CFTR | c.2254A>C (p.Ile752Leu) c.*1968A>C (n.*1968A>C) c.2071A>C (p.Ile691Leu) c.*554A>C (n.*554A>C) c.*2078A>C (n.*2078A>C) c.1828A>C (p.Ile610Leu) c.1402-10405A>C (n.1402-10405A>C) c.2164A>C (p.Ile722Leu) c.2344A>C (p.Ile782Leu) c.2011A>C (p.Ile671Leu) | ClinVar gnomAD v4 |
7 | g.117592421A>G | CA368980653 | CFTR | c.2254A>G (p.Ile752Val) c.*1968A>G (n.*1968A>G) c.2071A>G (p.Ile691Val) c.*554A>G (n.*554A>G) c.*2078A>G (n.*2078A>G) c.1828A>G (p.Ile610Val) c.1402-10405A>G (n.1402-10405A>G) c.2164A>G (p.Ile722Val) c.2344A>G (p.Ile782Val) c.2011A>G (p.Ile671Val) | |
7 | g.117592421A>T | CA368980656 | CFTR | c.2254A>T (p.Ile752Phe) c.*1968A>T (n.*1968A>T) c.2071A>T (p.Ile691Phe) c.*554A>T (n.*554A>T) c.*2078A>T (n.*2078A>T) c.1828A>T (p.Ile610Phe) c.1402-10405A>T (n.1402-10405A>T) c.2164A>T (p.Ile722Phe) c.2344A>T (p.Ile782Phe) c.2011A>T (p.Ile671Phe) | ClinVar |
7 | g.117592422T>A | CA368980663 | CFTR | c.2255T>A (p.Ile752Asn) c.*1969T>A (n.*1969T>A) c.2072T>A (p.Ile691Asn) c.*555T>A (n.*555T>A) c.*2079T>A (n.*2079T>A) c.1829T>A (p.Ile610Asn) c.1402-10404T>A (n.1402-10404T>A) c.2165T>A (p.Ile722Asn) c.2345T>A (p.Ile782Asn) c.2012T>A (p.Ile671Asn) | |
7 | g.117592422T>C | CA368980666 | CFTR | c.2255T>C (p.Ile752Thr) c.*1969T>C (n.*1969T>C) c.2072T>C (p.Ile691Thr) c.*555T>C (n.*555T>C) c.*2079T>C (n.*2079T>C) c.1829T>C (p.Ile610Thr) c.1402-10404T>C (n.1402-10404T>C) c.2165T>C (p.Ile722Thr) c.2345T>C (p.Ile782Thr) c.2012T>C (p.Ile671Thr) | dbSNP |
7 | g.117592422T>G | CA4451162 | CFTR | c.2255T>G (p.Ile752Ser) c.*1969T>G (n.*1969T>G) c.2072T>G (p.Ile691Ser) c.*555T>G (n.*555T>G) c.*2079T>G (n.*2079T>G) c.1829T>G (p.Ile610Ser) c.1402-10404T>G (n.1402-10404T>G) c.2165T>G (p.Ile722Ser) c.2345T>G (p.Ile782Ser) c.2012T>G (p.Ile671Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.117592422T= | CA1737395114 | CFTR | c.2255T= (p.Ile752=) c.*1969T= (n.*1969T=) c.2072T= (p.Ile691=) c.*555T= (n.*555T=) c.*2079T= (n.*2079T=) c.1829T= (p.Ile610=) c.1402-10404T= (n.1402-10404T=) c.2165T= (p.Ile722=) c.2345T= (p.Ile782=) c.2012T= (p.Ile671=) | |
7 | g.117592423C>A | CA457449566 | CFTR | c.2256C>A (p.Ile752=) c.*1970C>A (n.*1970C>A) c.2073C>A (p.Ile691=) c.*556C>A (n.*556C>A) c.*2080C>A (n.*2080C>A) c.1830C>A (p.Ile610=) c.1402-10403C>A (n.1402-10403C>A) c.2166C>A (p.Ile722=) c.2346C>A (p.Ile782=) c.2013C>A (p.Ile671=) | gnomAD v4 |
7 | g.117592423C>G | CA368980670 | CFTR | c.2256C>G (p.Ile752Met) c.*1970C>G (n.*1970C>G) c.2073C>G (p.Ile691Met) c.*556C>G (n.*556C>G) c.*2080C>G (n.*2080C>G) c.1830C>G (p.Ile610Met) c.1402-10403C>G (n.1402-10403C>G) c.2166C>G (p.Ile722Met) c.2346C>G (p.Ile782Met) c.2013C>G (p.Ile671Met) | |
7 | g.117592423C>T | CA457449569 | CFTR | c.2256C>T (p.Ile752=) c.*1970C>T (n.*1970C>T) c.2073C>T (p.Ile691=) c.*556C>T (n.*556C>T) c.*2080C>T (n.*2080C>T) c.1830C>T (p.Ile610=) c.1402-10403C>T (n.1402-10403C>T) c.2166C>T (p.Ile722=) c.2346C>T (p.Ile782=) c.2013C>T (p.Ile671=) | |
7 | g.117592424A= | CA1737395123 | CFTR | c.2257A= (p.Ser753=) c.*1971A= (n.*1971A=) c.2074A= (p.Ser692=) c.*557A= (n.*557A=) c.*2081A= (n.*2081A=) c.1831A= (p.Ser611=) c.1402-10402A= (n.1402-10402A=) c.2167A= (p.Ser723=) c.2347A= (p.Ser783=) c.2014A= (p.Ser672=) | |
7 | g.117592424A>C | CA368980673 | CFTR | c.2257A>C (p.Ser753Arg) c.*1971A>C (n.*1971A>C) c.2074A>C (p.Ser692Arg) c.*557A>C (n.*557A>C) c.*2081A>C (n.*2081A>C) c.1831A>C (p.Ser611Arg) c.1402-10402A>C (n.1402-10402A>C) c.2167A>C (p.Ser723Arg) c.2347A>C (p.Ser783Arg) c.2014A>C (p.Ser672Arg) | |
7 | g.117592424A>G | CA368980675 | CFTR | c.2257A>G (p.Ser753Gly) c.*1971A>G (n.*1971A>G) c.2074A>G (p.Ser692Gly) c.*557A>G (n.*557A>G) c.*2081A>G (n.*2081A>G) c.1831A>G (p.Ser611Gly) c.1402-10402A>G (n.1402-10402A>G) c.2167A>G (p.Ser723Gly) c.2347A>G (p.Ser783Gly) c.2014A>G (p.Ser672Gly) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.117592424A>T | CA368980676 | CFTR | c.2257A>T (p.Ser753Cys) c.*1971A>T (n.*1971A>T) c.2074A>T (p.Ser692Cys) c.*557A>T (n.*557A>T) c.*2081A>T (n.*2081A>T) c.1831A>T (p.Ser611Cys) c.1402-10402A>T (n.1402-10402A>T) c.2167A>T (p.Ser723Cys) c.2347A>T (p.Ser783Cys) c.2014A>T (p.Ser672Cys) | |
7 | g.117592425G>A | CA4451163 | CFTR | c.2258G>A (p.Ser753Asn) c.*1972G>A (n.*1972G>A) c.2075G>A (p.Ser692Asn) c.*558G>A (n.*558G>A) c.*2082G>A (n.*2082G>A) c.1832G>A (p.Ser611Asn) c.1402-10401G>A (n.1402-10401G>A) c.2168G>A (p.Ser723Asn) c.2348G>A (p.Ser783Asn) c.2015G>A (p.Ser672Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.117592425G>C | CA368980681 | CFTR | c.2258G>C (p.Ser753Thr) c.*1972G>C (n.*1972G>C) c.2075G>C (p.Ser692Thr) c.*558G>C (n.*558G>C) c.*2082G>C (n.*2082G>C) c.1832G>C (p.Ser611Thr) c.1402-10401G>C (n.1402-10401G>C) c.2168G>C (p.Ser723Thr) c.2348G>C (p.Ser783Thr) c.2015G>C (p.Ser672Thr) | gnomAD v4 |
7 | g.117592425G= | CA1737395126 | CFTR | c.2258G= (p.Ser753=) c.*1972G= (n.*1972G=) c.2075G= (p.Ser692=) c.*558G= (n.*558G=) c.*2082G= (n.*2082G=) c.1832G= (p.Ser611=) c.1402-10401G= (n.1402-10401G=) c.2168G= (p.Ser723=) c.2348G= (p.Ser783=) c.2015G= (p.Ser672=) | |
7 | g.117592425G>T | CA368980683 | CFTR | c.2258G>T (p.Ser753Ile) c.*1972G>T (n.*1972G>T) c.2075G>T (p.Ser692Ile) c.*558G>T (n.*558G>T) c.*2082G>T (n.*2082G>T) c.1832G>T (p.Ser611Ile) c.1402-10401G>T (n.1402-10401G>T) c.2168G>T (p.Ser723Ile) c.2348G>T (p.Ser783Ile) c.2015G>T (p.Ser672Ile) | |
7 | g.117592426C>A | CA368980689 | CFTR | c.2259C>A (p.Ser753Arg) c.*1973C>A (n.*1973C>A) c.2076C>A (p.Ser692Arg) c.*559C>A (n.*559C>A) c.*2083C>A (n.*2083C>A) c.1833C>A (p.Ser611Arg) c.1402-10400C>A (n.1402-10400C>A) c.2169C>A (p.Ser723Arg) c.2349C>A (p.Ser783Arg) c.2016C>A (p.Ser672Arg) | |
7 | g.117592426C= | CA1737395133 | CFTR | c.2259C= (p.Ser753=) c.*1973C= (n.*1973C=) c.2076C= (p.Ser692=) c.*559C= (n.*559C=) c.*2083C= (n.*2083C=) c.1833C= (p.Ser611=) c.1402-10400C= (n.1402-10400C=) c.2169C= (p.Ser723=) c.2349C= (p.Ser783=) c.2016C= (p.Ser672=) | |
7 | g.117592426C>G | CA326780 | CFTR | c.2259C>G (p.Ser753Arg) c.*1973C>G (n.*1973C>G) c.2076C>G (p.Ser692Arg) c.*559C>G (n.*559C>G) c.*2083C>G (n.*2083C>G) c.1833C>G (p.Ser611Arg) c.1402-10400C>G (n.1402-10400C>G) c.2169C>G (p.Ser723Arg) c.2349C>G (p.Ser783Arg) c.2016C>G (p.Ser672Arg) | ClinVar dbSNP |
7 | g.117592426C>T | CA326782 | CFTR | c.2259C>T (p.Ser753=) c.*1973C>T (n.*1973C>T) c.2076C>T (p.Ser692=) c.*559C>T (n.*559C>T) c.*2083C>T (n.*2083C>T) c.1833C>T (p.Ser611=) c.1402-10400C>T (n.1402-10400C>T) c.2169C>T (p.Ser723=) c.2349C>T (p.Ser783=) c.2016C>T (p.Ser672=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.117592427G>A | CA326784 | CFTR | c.2260G>A (p.Val754Met) c.*1974G>A (n.*1974G>A) c.2077G>A (p.Val693Met) c.*560G>A (n.*560G>A) c.*2084G>A (n.*2084G>A) c.1834G>A (p.Val612Met) c.1402-10399G>A (n.1402-10399G>A) c.2170G>A (p.Val724Met) c.2350G>A (p.Val784Met) c.2017G>A (p.Val673Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.117592427G>C | CA368980697 | CFTR | c.2260G>C (p.Val754Leu) c.*1974G>C (n.*1974G>C) c.2077G>C (p.Val693Leu) c.*560G>C (n.*560G>C) c.*2084G>C (n.*2084G>C) c.1834G>C (p.Val612Leu) c.1402-10399G>C (n.1402-10399G>C) c.2170G>C (p.Val724Leu) c.2350G>C (p.Val784Leu) c.2017G>C (p.Val673Leu) | |
7 | g.117592427G= | CA1737395143 | CFTR | c.2260G= (p.Val754=) c.*1974G= (n.*1974G=) c.2077G= (p.Val693=) c.*560G= (n.*560G=) c.*2084G= (n.*2084G=) c.1834G= (p.Val612=) c.1402-10399G= (n.1402-10399G=) c.2170G= (p.Val724=) c.2350G= (p.Val784=) c.2017G= (p.Val673=) | |
7 | g.117592427G>T | CA368980696 | CFTR | c.2260G>T (p.Val754Leu) c.*1974G>T (n.*1974G>T) c.2077G>T (p.Val693Leu) c.*560G>T (n.*560G>T) c.*2084G>T (n.*2084G>T) c.1834G>T (p.Val612Leu) c.1402-10399G>T (n.1402-10399G>T) c.2170G>T (p.Val724Leu) c.2350G>T (p.Val784Leu) c.2017G>T (p.Val673Leu) | dbSNP |
7 | g.117592428del | CA2573141691 | CFTR | c.2261del (p.Val754GlyfsTer17) c.*1975del (n.*1975del) c.2078del (p.Val693GlyfsTer17) c.*561del (n.*561del) c.*2085del (n.*2085del) c.1835del (p.Val612GlyfsTer17) c.1402-10398del (n.1402-10398del) c.2171del (p.Val724GlyfsTer17) c.2351del (p.Val784GlyfsTer17) c.2018del (p.Val673GlyfsTer17) | ClinVar dbSNP |
7 | g.117592428T>A | CA368980701 | CFTR | c.2261T>A (p.Val754Glu) c.*1975T>A (n.*1975T>A) c.2078T>A (p.Val693Glu) c.*561T>A (n.*561T>A) c.*2085T>A (n.*2085T>A) c.1835T>A (p.Val612Glu) c.1402-10398T>A (n.1402-10398T>A) c.2171T>A (p.Val724Glu) c.2351T>A (p.Val784Glu) c.2018T>A (p.Val673Glu) | |
7 | g.117592428T>C | CA368980703 | CFTR | c.2261T>C (p.Val754Ala) c.*1975T>C (n.*1975T>C) c.2078T>C (p.Val693Ala) c.*561T>C (n.*561T>C) c.*2085T>C (n.*2085T>C) c.1835T>C (p.Val612Ala) c.1402-10398T>C (n.1402-10398T>C) c.2171T>C (p.Val724Ala) c.2351T>C (p.Val784Ala) c.2018T>C (p.Val673Ala) | |
7 | g.117592428T>G | CA368980705 | CFTR | c.2261T>G (p.Val754Gly) c.*1975T>G (n.*1975T>G) c.2078T>G (p.Val693Gly) c.*561T>G (n.*561T>G) c.*2085T>G (n.*2085T>G) c.1835T>G (p.Val612Gly) c.1402-10398T>G (n.1402-10398T>G) c.2171T>G (p.Val724Gly) c.2351T>G (p.Val784Gly) c.2018T>G (p.Val673Gly) | |
7 | g.117592429G>A | CA457449578 | CFTR | c.2262G>A (p.Val754=) c.*1976G>A (n.*1976G>A) c.2079G>A (p.Val693=) c.*562G>A (n.*562G>A) c.*2086G>A (n.*2086G>A) c.1836G>A (p.Val612=) c.1402-10397G>A (n.1402-10397G>A) c.2172G>A (p.Val724=) c.2352G>A (p.Val784=) c.2019G>A (p.Val673=) | COSMIC |
7 | g.117592429G>C | CA457449574 | CFTR | c.2262G>C (p.Val754=) c.*1976G>C (n.*1976G>C) c.2079G>C (p.Val693=) c.*562G>C (n.*562G>C) c.*2086G>C (n.*2086G>C) c.1836G>C (p.Val612=) c.1402-10397G>C (n.1402-10397G>C) c.2172G>C (p.Val724=) c.2352G>C (p.Val784=) c.2019G>C (p.Val673=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.117592429G= | CA1737395150 | CFTR | c.2262G= (p.Val754=) c.*1976G= (n.*1976G=) c.2079G= (p.Val693=) c.*562G= (n.*562G=) c.*2086G= (n.*2086G=) c.1836G= (p.Val612=) c.1402-10397G= (n.1402-10397G=) c.2172G= (p.Val724=) c.2352G= (p.Val784=) c.2019G= (p.Val673=) | |
7 | g.117592429G>T | CA457449575 | CFTR | c.2262G>T (p.Val754=) c.*1976G>T (n.*1976G>T) c.2079G>T (p.Val693=) c.*562G>T (n.*562G>T) c.*2086G>T (n.*2086G>T) c.1836G>T (p.Val612=) c.1402-10397G>T (n.1402-10397G>T) c.2172G>T (p.Val724=) c.2352G>T (p.Val784=) c.2019G>T (p.Val673=) | ClinVar |
7 | g.117592430A= | CA1737395154 | CFTR | c.2263A= (p.Ile755=) c.*1977A= (n.*1977A=) c.2080A= (p.Ile694=) c.*563A= (n.*563A=) c.*2087A= (n.*2087A=) c.1837A= (p.Ile613=) c.1402-10396A= (n.1402-10396A=) c.2173A= (p.Ile725=) c.2353A= (p.Ile785=) c.2020A= (p.Ile674=) | |
7 | g.117592430A>C | CA368980710 | CFTR | c.2263A>C (p.Ile755Leu) c.*1977A>C (n.*1977A>C) c.2080A>C (p.Ile694Leu) c.*563A>C (n.*563A>C) c.*2087A>C (n.*2087A>C) c.1837A>C (p.Ile613Leu) c.1402-10396A>C (n.1402-10396A>C) c.2173A>C (p.Ile725Leu) c.2353A>C (p.Ile785Leu) c.2020A>C (p.Ile674Leu) | |
7 | g.117592430A>G | CA368980715 | CFTR | c.2263A>G (p.Ile755Val) c.*1977A>G (n.*1977A>G) c.2080A>G (p.Ile694Val) c.*563A>G (n.*563A>G) c.*2087A>G (n.*2087A>G) c.1837A>G (p.Ile613Val) c.1402-10396A>G (n.1402-10396A>G) c.2173A>G (p.Ile725Val) c.2353A>G (p.Ile785Val) c.2020A>G (p.Ile674Val) | |
7 | g.117592430A>T | CA4451164 | CFTR | c.2263A>T (p.Ile755Phe) c.*1977A>T (n.*1977A>T) c.2080A>T (p.Ile694Phe) c.*563A>T (n.*563A>T) c.*2087A>T (n.*2087A>T) c.1837A>T (p.Ile613Phe) c.1402-10396A>T (n.1402-10396A>T) c.2173A>T (p.Ile725Phe) c.2353A>T (p.Ile785Phe) c.2020A>T (p.Ile674Phe) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.117592431T>A | CA368980718 | CFTR | c.2264T>A (p.Ile755Asn) c.*1978T>A (n.*1978T>A) c.2081T>A (p.Ile694Asn) c.*564T>A (n.*564T>A) c.*2088T>A (n.*2088T>A) c.1838T>A (p.Ile613Asn) c.1402-10395T>A (n.1402-10395T>A) c.2174T>A (p.Ile725Asn) c.2354T>A (p.Ile785Asn) c.2021T>A (p.Ile674Asn) | |
7 | g.117592431T>C | CA368980720 | CFTR | c.2264T>C (p.Ile755Thr) c.*1978T>C (n.*1978T>C) c.2081T>C (p.Ile694Thr) c.*564T>C (n.*564T>C) c.*2088T>C (n.*2088T>C) c.1838T>C (p.Ile613Thr) c.1402-10395T>C (n.1402-10395T>C) c.2174T>C (p.Ile725Thr) c.2354T>C (p.Ile785Thr) c.2021T>C (p.Ile674Thr) | |
7 | g.117592431T>G | CA368980723 | CFTR | c.2264T>G (p.Ile755Ser) c.*1978T>G (n.*1978T>G) c.2081T>G (p.Ile694Ser) c.*564T>G (n.*564T>G) c.*2088T>G (n.*2088T>G) c.1838T>G (p.Ile613Ser) c.1402-10395T>G (n.1402-10395T>G) c.2174T>G (p.Ile725Ser) c.2354T>G (p.Ile785Ser) c.2021T>G (p.Ile674Ser) | |
7 | g.117592432C>A | CA457449584 | CFTR | c.2265C>A (p.Ile755=) c.*1979C>A (n.*1979C>A) c.2082C>A (p.Ile694=) c.*565C>A (n.*565C>A) c.*2089C>A (n.*2089C>A) c.1839C>A (p.Ile613=) c.1402-10394C>A (n.1402-10394C>A) c.2175C>A (p.Ile725=) c.2355C>A (p.Ile785=) c.2022C>A (p.Ile674=) | |
7 | g.117592432C>G | CA368980725 | CFTR | c.2265C>G (p.Ile755Met) c.*1979C>G (n.*1979C>G) c.2082C>G (p.Ile694Met) c.*565C>G (n.*565C>G) c.*2089C>G (n.*2089C>G) c.1839C>G (p.Ile613Met) c.1402-10394C>G (n.1402-10394C>G) c.2175C>G (p.Ile725Met) c.2355C>G (p.Ile785Met) c.2022C>G (p.Ile674Met) | |
7 | g.117592432C>T | CA457449586 | CFTR | c.2265C>T (p.Ile755=) c.*1979C>T (n.*1979C>T) c.2082C>T (p.Ile694=) c.*565C>T (n.*565C>T) c.*2089C>T (n.*2089C>T) c.1839C>T (p.Ile613=) c.1402-10394C>T (n.1402-10394C>T) c.2175C>T (p.Ile725=) c.2355C>T (p.Ile785=) c.2022C>T (p.Ile674=) | |
7 | g.117592433A= | CA1737395157 | CFTR | c.2266A= (p.Ser756=) c.*1980A= (n.*1980A=) c.2083A= (p.Ser695=) c.*566A= (n.*566A=) c.*2090A= (n.*2090A=) c.1840A= (p.Ser614=) c.1402-10393A= (n.1402-10393A=) c.2176A= (p.Ser726=) c.2356A= (p.Ser786=) c.2023A= (p.Ser675=) | |
7 | g.117592433A>C | CA368980729 | CFTR | c.2266A>C (p.Ser756Arg) c.*1980A>C (n.*1980A>C) c.2083A>C (p.Ser695Arg) c.*566A>C (n.*566A>C) c.*2090A>C (n.*2090A>C) c.1840A>C (p.Ser614Arg) c.1402-10393A>C (n.1402-10393A>C) c.2176A>C (p.Ser726Arg) c.2356A>C (p.Ser786Arg) c.2023A>C (p.Ser675Arg) | |
7 | g.117592433A>G | CA368980730 | CFTR | c.2266A>G (p.Ser756Gly) c.*1980A>G (n.*1980A>G) c.2083A>G (p.Ser695Gly) c.*566A>G (n.*566A>G) c.*2090A>G (n.*2090A>G) c.1840A>G (p.Ser614Gly) c.1402-10393A>G (n.1402-10393A>G) c.2176A>G (p.Ser726Gly) c.2356A>G (p.Ser786Gly) c.2023A>G (p.Ser675Gly) | |
7 | g.117592433A>T | CA368980732 | CFTR | c.2266A>T (p.Ser756Cys) c.*1980A>T (n.*1980A>T) c.2083A>T (p.Ser695Cys) c.*566A>T (n.*566A>T) c.*2090A>T (n.*2090A>T) c.1840A>T (p.Ser614Cys) c.1402-10393A>T (n.1402-10393A>T) c.2176A>T (p.Ser726Cys) c.2356A>T (p.Ser786Cys) c.2023A>T (p.Ser675Cys) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.117592434G>A | CA368980736 | CFTR | c.2267G>A (p.Ser756Asn) c.*1981G>A (n.*1981G>A) c.2084G>A (p.Ser695Asn) c.*567G>A (n.*567G>A) c.*2091G>A (n.*2091G>A) c.1841G>A (p.Ser614Asn) c.1402-10392G>A (n.1402-10392G>A) c.2177G>A (p.Ser726Asn) c.2357G>A (p.Ser786Asn) c.2024G>A (p.Ser675Asn) | ClinVar gnomAD v4 |
7 | g.117592434G>C | CA368980741 | CFTR | c.2267G>C (p.Ser756Thr) c.*1981G>C (n.*1981G>C) c.2084G>C (p.Ser695Thr) c.*567G>C (n.*567G>C) c.*2091G>C (n.*2091G>C) c.1841G>C (p.Ser614Thr) c.1402-10392G>C (n.1402-10392G>C) c.2177G>C (p.Ser726Thr) c.2357G>C (p.Ser786Thr) c.2024G>C (p.Ser675Thr) | |
7 | g.117592434G>T | CA368980738 | CFTR | c.2267G>T (p.Ser756Ile) c.*1981G>T (n.*1981G>T) c.2084G>T (p.Ser695Ile) c.*567G>T (n.*567G>T) c.*2091G>T (n.*2091G>T) c.1841G>T (p.Ser614Ile) c.1402-10392G>T (n.1402-10392G>T) c.2177G>T (p.Ser726Ile) c.2357G>T (p.Ser786Ile) c.2024G>T (p.Ser675Ile) | ClinVar gnomAD v4 |
7 | g.117592435C>A | CA368980744 | CFTR | c.2268C>A (p.Ser756Arg) c.*1982C>A (n.*1982C>A) c.2085C>A (p.Ser695Arg) c.*568C>A (n.*568C>A) c.*2092C>A (n.*2092C>A) c.1842C>A (p.Ser614Arg) c.1402-10391C>A (n.1402-10391C>A) c.2178C>A (p.Ser726Arg) c.2358C>A (p.Ser786Arg) c.2025C>A (p.Ser675Arg) | |
7 | g.117592435C>G | CA368980746 | CFTR | c.2268C>G (p.Ser756Arg) c.*1982C>G (n.*1982C>G) c.2085C>G (p.Ser695Arg) c.*568C>G (n.*568C>G) c.*2092C>G (n.*2092C>G) c.1842C>G (p.Ser614Arg) c.1402-10391C>G (n.1402-10391C>G) c.2178C>G (p.Ser726Arg) c.2358C>G (p.Ser786Arg) c.2025C>G (p.Ser675Arg) | |
7 | g.117592435C>T | CA457449598 | CFTR | c.2268C>T (p.Ser756=) c.*1982C>T (n.*1982C>T) c.2085C>T (p.Ser695=) c.*568C>T (n.*568C>T) c.*2092C>T (n.*2092C>T) c.1842C>T (p.Ser614=) c.1402-10391C>T (n.1402-10391C>T) c.2178C>T (p.Ser726=) c.2358C>T (p.Ser786=) c.2025C>T (p.Ser675=) | |
7 | g.117592436A= | CA1737395159 | CFTR | c.2269A= (p.Thr757=) c.*1983A= (n.*1983A=) c.2086A= (p.Thr696=) c.*569A= (n.*569A=) c.*2093A= (n.*2093A=) c.1843A= (p.Thr615=) c.1402-10390A= (n.1402-10390A=) c.2179A= (p.Thr727=) c.2359A= (p.Thr787=) c.2026A= (p.Thr676=) | |
7 | g.117592436A>C | CA368980750 | CFTR | c.2269A>C (p.Thr757Pro) c.*1983A>C (n.*1983A>C) c.2086A>C (p.Thr696Pro) c.*569A>C (n.*569A>C) c.*2093A>C (n.*2093A>C) c.1843A>C (p.Thr615Pro) c.1402-10390A>C (n.1402-10390A>C) c.2179A>C (p.Thr727Pro) c.2359A>C (p.Thr787Pro) c.2026A>C (p.Thr676Pro) | |
7 | g.117592436A>G | CA368980751 | CFTR | c.2269A>G (p.Thr757Ala) c.*1983A>G (n.*1983A>G) c.2086A>G (p.Thr696Ala) c.*569A>G (n.*569A>G) c.*2093A>G (n.*2093A>G) c.1843A>G (p.Thr615Ala) c.1402-10390A>G (n.1402-10390A>G) c.2179A>G (p.Thr727Ala) c.2359A>G (p.Thr787Ala) c.2026A>G (p.Thr676Ala) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.117592436A>T | CA368980753 | CFTR | c.2269A>T (p.Thr757Ser) c.*1983A>T (n.*1983A>T) c.2086A>T (p.Thr696Ser) c.*569A>T (n.*569A>T) c.*2093A>T (n.*2093A>T) c.1843A>T (p.Thr615Ser) c.1402-10390A>T (n.1402-10390A>T) c.2179A>T (p.Thr727Ser) c.2359A>T (p.Thr787Ser) c.2026A>T (p.Thr676Ser) | |
7 | g.117592437C>A | CA368980754 | CFTR | c.2270C>A (p.Thr757Asn) c.*1984C>A (n.*1984C>A) c.2087C>A (p.Thr696Asn) c.*570C>A (n.*570C>A) c.*2094C>A (n.*2094C>A) c.1844C>A (p.Thr615Asn) c.1402-10389C>A (n.1402-10389C>A) c.2180C>A (p.Thr727Asn) c.2360C>A (p.Thr787Asn) c.2027C>A (p.Thr676Asn) | |
7 | g.117592437C= | CA1737395161 | CFTR | c.2270C= (p.Thr757=) c.*1984C= (n.*1984C=) c.2087C= (p.Thr696=) c.*570C= (n.*570C=) c.*2094C= (n.*2094C=) c.1844C= (p.Thr615=) c.1402-10389C= (n.1402-10389C=) c.2180C= (p.Thr727=) c.2360C= (p.Thr787=) c.2027C= (p.Thr676=) | |
7 | g.117592437C>G | CA368980756 | CFTR | c.2270C>G (p.Thr757Ser) c.*1984C>G (n.*1984C>G) c.2087C>G (p.Thr696Ser) c.*570C>G (n.*570C>G) c.*2094C>G (n.*2094C>G) c.1844C>G (p.Thr615Ser) c.1402-10389C>G (n.1402-10389C>G) c.2180C>G (p.Thr727Ser) c.2360C>G (p.Thr787Ser) c.2027C>G (p.Thr676Ser) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
7 | g.117592437C>T | CA368980758 | CFTR | c.2270C>T (p.Thr757Ile) c.*1984C>T (n.*1984C>T) c.2087C>T (p.Thr696Ile) c.*570C>T (n.*570C>T) c.*2094C>T (n.*2094C>T) c.1844C>T (p.Thr615Ile) c.1402-10389C>T (n.1402-10389C>T) c.2180C>T (p.Thr727Ile) c.2360C>T (p.Thr787Ile) c.2027C>T (p.Thr676Ile) | ClinVar |
7 | g.117592438T>A | CA457449605 | CFTR | c.2271T>A (p.Thr757=) c.*1985T>A (n.*1985T>A) c.2088T>A (p.Thr696=) c.*571T>A (n.*571T>A) c.*2095T>A (n.*2095T>A) c.1845T>A (p.Thr615=) c.1402-10388T>A (n.1402-10388T>A) c.2181T>A (p.Thr727=) c.2361T>A (p.Thr787=) c.2028T>A (p.Thr676=) | |
7 | g.117592438T>C | CA457449608 | CFTR | c.2271T>C (p.Thr757=) c.*1985T>C (n.*1985T>C) c.2088T>C (p.Thr696=) c.*571T>C (n.*571T>C) c.*2095T>C (n.*2095T>C) c.1845T>C (p.Thr615=) c.1402-10388T>C (n.1402-10388T>C) c.2181T>C (p.Thr727=) c.2361T>C (p.Thr787=) c.2028T>C (p.Thr676=) | |
7 | g.117592438T>G | CA457449609 | CFTR | c.2271T>G (p.Thr757=) c.*1985T>G (n.*1985T>G) c.2088T>G (p.Thr696=) c.*571T>G (n.*571T>G) c.*2095T>G (n.*2095T>G) c.1845T>G (p.Thr615=) c.1402-10388T>G (n.1402-10388T>G) c.2181T>G (p.Thr727=) c.2361T>G (p.Thr787=) c.2028T>G (p.Thr676=) | |
7 | g.117592439G>A | CA368980761 | CFTR | c.2272G>A (p.Gly758Ser) c.*1986G>A (n.*1986G>A) c.2089G>A (p.Gly697Ser) c.*572G>A (n.*572G>A) c.*2096G>A (n.*2096G>A) c.1846G>A (p.Gly616Ser) c.1402-10387G>A (n.1402-10387G>A) c.2182G>A (p.Gly728Ser) c.2362G>A (p.Gly788Ser) c.2029G>A (p.Gly677Ser) | |
7 | g.117592439G>C | CA368980763 | CFTR | c.2272G>C (p.Gly758Arg) c.*1986G>C (n.*1986G>C) c.2089G>C (p.Gly697Arg) c.*572G>C (n.*572G>C) c.*2096G>C (n.*2096G>C) c.1846G>C (p.Gly616Arg) c.1402-10387G>C (n.1402-10387G>C) c.2182G>C (p.Gly728Arg) c.2362G>C (p.Gly788Arg) c.2029G>C (p.Gly677Arg) | |
7 | g.117592439G>T | CA368980765 | CFTR | c.2272G>T (p.Gly758Cys) c.*1986G>T (n.*1986G>T) c.2089G>T (p.Gly697Cys) c.*572G>T (n.*572G>T) c.*2096G>T (n.*2096G>T) c.1846G>T (p.Gly616Cys) c.1402-10387G>T (n.1402-10387G>T) c.2182G>T (p.Gly728Cys) c.2362G>T (p.Gly788Cys) c.2029G>T (p.Gly677Cys) | |
7 | g.117592440G>A | CA368980770 | CFTR | c.2273G>A (p.Gly758Asp) c.*1987G>A (n.*1987G>A) c.2090G>A (p.Gly697Asp) c.*573G>A (n.*573G>A) c.*2097G>A (n.*2097G>A) c.1847G>A (p.Gly616Asp) c.1402-10386G>A (n.1402-10386G>A) c.2183G>A (p.Gly728Asp) c.2363G>A (p.Gly788Asp) c.2030G>A (p.Gly677Asp) | |
7 | g.117592440G>C | CA368980773 | CFTR | c.2273G>C (p.Gly758Ala) c.*1987G>C (n.*1987G>C) c.2090G>C (p.Gly697Ala) c.*573G>C (n.*573G>C) c.*2097G>C (n.*2097G>C) c.1847G>C (p.Gly616Ala) c.1402-10386G>C (n.1402-10386G>C) c.2183G>C (p.Gly728Ala) c.2363G>C (p.Gly788Ala) c.2030G>C (p.Gly677Ala) | |
7 | g.117592440G>T | CA368980768 | CFTR | c.2273G>T (p.Gly758Val) c.*1987G>T (n.*1987G>T) c.2090G>T (p.Gly697Val) c.*573G>T (n.*573G>T) c.*2097G>T (n.*2097G>T) c.1847G>T (p.Gly616Val) c.1402-10386G>T (n.1402-10386G>T) c.2183G>T (p.Gly728Val) c.2363G>T (p.Gly788Val) c.2030G>T (p.Gly677Val) | |
7 | g.117592440_117592442delinsGCC | CA1737395164 | CFTR | c.2273_2275delinsGCC (p.Gly758=) c.*1987_*1989delinsGCC (n.*1987_*1989delinsGCC) c.2090_2092delinsGCC (p.Gly697=) c.*573_*575delinsGCC (n.*573_*575delinsGCC) c.*2097_*2099delinsGCC (n.*2097_*2099delinsGCC) c.1847_1849delinsGCC (p.Gly616=) c.1402-10386_1402-10384delinsGCC (n.1402-10386_1402-10384delinsGCC) c.2183_2185delinsGCC (p.Gly728=) c.2363_2365delinsGCC (p.Gly788=) c.2030_2032delinsGCC (p.Gly677=) | |
7 | g.117592440_117592456delinsGCCCCACGCTTCAGGCA | CA1737395165 | CFTR | c.2273_2289delinsGCCCCACGCTTCAGGCA (p.Gly758=) c.*1987_*2003delinsGCCCCACGCTTCAGGCA (n.*1987_*2003delinsGCCCCACGCTTCAGGCA) c.2090_2106delinsGCCCCACGCTTCAGGCA (p.Gly697=) c.*573_*589delinsGCCCCACGCTTCAGGCA (n.*573_*589delinsGCCCCACGCTTCAGGCA) c.*2097_*2113delinsGCCCCACGCTTCAGGCA (n.*2097_*2113delinsGCCCCACGCTTCAGGCA) c.1847_1863delinsGCCCCACGCTTCAGGCA (p.Gly616=) c.1402-10386_1402-10370delinsGCCCCACGCTTCAGGCA (n.1402-10386_1402-10370delinsGCCCCACGCTTCAGGCA) c.2183_2199delinsGCCCCACGCTTCAGGCA (p.Gly728=) c.2363_2379delinsGCCCCACGCTTCAGGCA (p.Gly788=) c.2030_2046delinsGCCCCACGCTTCAGGCA (p.Gly677=) | |
7 | g.117592441C>A | CA457449610 | CFTR | c.2274C>A (p.Gly758=) c.*1988C>A (n.*1988C>A) c.2091C>A (p.Gly697=) c.*574C>A (n.*574C>A) c.*2098C>A (n.*2098C>A) c.1848C>A (p.Gly616=) c.1402-10385C>A (n.1402-10385C>A) c.2184C>A (p.Gly728=) c.2364C>A (p.Gly788=) c.2031C>A (p.Gly677=) | gnomAD v4 |
7 | g.117592441C>G | CA457449612 | CFTR | c.2274C>G (p.Gly758=) c.*1988C>G (n.*1988C>G) c.2091C>G (p.Gly697=) c.*574C>G (n.*574C>G) c.*2098C>G (n.*2098C>G) c.1848C>G (p.Gly616=) c.1402-10385C>G (n.1402-10385C>G) c.2184C>G (p.Gly728=) c.2364C>G (p.Gly788=) c.2031C>G (p.Gly677=) | |
7 | g.117592441C>T | CA457449613 | CFTR | c.2274C>T (p.Gly758=) c.*1988C>T (n.*1988C>T) c.2091C>T (p.Gly697=) c.*574C>T (n.*574C>T) c.*2098C>T (n.*2098C>T) c.1848C>T (p.Gly616=) c.1402-10385C>T (n.1402-10385C>T) c.2184C>T (p.Gly728=) c.2364C>T (p.Gly788=) c.2031C>T (p.Gly677=) | |
7 | g.117592443_117592444del | CA326785 | CFTR | c.2276_2277del (p.Pro759HisfsTer19) c.*1990_*1991del (n.*1990_*1991del) c.2093_2094del (p.Pro698HisfsTer19) c.*576_*577del (n.*576_*577del) c.*2100_*2101del (n.*2100_*2101del) c.1850_1851del (p.Pro617HisfsTer19) c.1402-10383_1402-10382del (n.1402-10383_1402-10382del) c.2186_2187del (p.Pro729HisfsTer19) c.2366_2367del (p.Pro789HisfsTer19) c.2033_2034del (p.Pro678HisfsTer19) | dbSNP |
7 | g.117592442_117592457del | CA577680772 | CFTR | c.2275_2290del (p.Pro759GlufsTer7) c.*1989_*2004del (n.*1989_*2004del) c.2092_2107del (p.Pro698GlufsTer7) c.*575_*590del (n.*575_*590del) c.*2099_*2114del (n.*2099_*2114del) c.1849_1864del (p.Pro617GlufsTer7) c.1402-10384_1402-10369del (n.1402-10384_1402-10369del) c.2185_2200del (p.Pro729GlufsTer7) c.2365_2380del (p.Pro789GlufsTer7) c.2032_2047del (p.Pro678GlufsTer7) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.117592442C>A | CA368980778 | CFTR | c.2275C>A (p.Pro759Thr) c.*1989C>A (n.*1989C>A) c.2092C>A (p.Pro698Thr) c.*575C>A (n.*575C>A) c.*2099C>A (n.*2099C>A) c.1849C>A (p.Pro617Thr) c.1402-10384C>A (n.1402-10384C>A) c.2185C>A (p.Pro729Thr) c.2365C>A (p.Pro789Thr) c.2032C>A (p.Pro678Thr) | ClinVar dbSNP |
7 | g.117592442C= | CA1737395168 | CFTR | c.2275C= (p.Pro759=) c.*1989C= (n.*1989C=) c.2092C= (p.Pro698=) c.*575C= (n.*575C=) c.*2099C= (n.*2099C=) c.1849C= (p.Pro617=) c.1402-10384C= (n.1402-10384C=) c.2185C= (p.Pro729=) c.2365C= (p.Pro789=) c.2032C= (p.Pro678=) | |
7 | g.117592442C>G | CA368980782 | CFTR | c.2275C>G (p.Pro759Ala) c.*1989C>G (n.*1989C>G) c.2092C>G (p.Pro698Ala) c.*575C>G (n.*575C>G) c.*2099C>G (n.*2099C>G) c.1849C>G (p.Pro617Ala) c.1402-10384C>G (n.1402-10384C>G) c.2185C>G (p.Pro729Ala) c.2365C>G (p.Pro789Ala) c.2032C>G (p.Pro678Ala) | |
7 | g.117592442C>T | CA368980780 | CFTR | c.2275C>T (p.Pro759Ser) c.*1989C>T (n.*1989C>T) c.2092C>T (p.Pro698Ser) c.*575C>T (n.*575C>T) c.*2099C>T (n.*2099C>T) c.1849C>T (p.Pro617Ser) c.1402-10384C>T (n.1402-10384C>T) c.2185C>T (p.Pro729Ser) c.2365C>T (p.Pro789Ser) c.2032C>T (p.Pro678Ser) | |
7 | g.117592443C>A | CA368980785 | CFTR | c.2276C>A (p.Pro759His) c.*1990C>A (n.*1990C>A) c.2093C>A (p.Pro698His) c.*576C>A (n.*576C>A) c.*2100C>A (n.*2100C>A) c.1850C>A (p.Pro617His) c.1402-10383C>A (n.1402-10383C>A) c.2186C>A (p.Pro729His) c.2366C>A (p.Pro789His) c.2033C>A (p.Pro678His) | |
7 | g.117592443C>G | CA368980788 | CFTR | c.2276C>G (p.Pro759Arg) c.*1990C>G (n.*1990C>G) c.2093C>G (p.Pro698Arg) c.*576C>G (n.*576C>G) c.*2100C>G (n.*2100C>G) c.1850C>G (p.Pro617Arg) c.1402-10383C>G (n.1402-10383C>G) c.2186C>G (p.Pro729Arg) c.2366C>G (p.Pro789Arg) c.2033C>G (p.Pro678Arg) | |
7 | g.117592443C>T | CA368980791 | CFTR | c.2276C>T (p.Pro759Leu) c.*1990C>T (n.*1990C>T) c.2093C>T (p.Pro698Leu) c.*576C>T (n.*576C>T) c.*2100C>T (n.*2100C>T) c.1850C>T (p.Pro617Leu) c.1402-10383C>T (n.1402-10383C>T) c.2186C>T (p.Pro729Leu) c.2366C>T (p.Pro789Leu) c.2033C>T (p.Pro678Leu) | |
7 | g.117592443_117592444insTGT | CA2684619361 | CFTR | c.2276_2277insTGT (p.Pro759_Thr760insVal) c.*1990_*1991insTGT (n.*1990_*1991insTGT) c.2093_2094insTGT (p.Pro698_Thr699insVal) c.*576_*577insTGT (n.*576_*577insTGT) c.*2100_*2101insTGT (n.*2100_*2101insTGT) c.1850_1851insTGT (p.Pro617_Thr618insVal) c.1402-10383_1402-10382insTGT (n.1402-10383_1402-10382insTGT) c.2186_2187insTGT (p.Pro729_Thr730insVal) c.2366_2367insTGT (p.Pro789_Thr790insVal) c.2033_2034insTGT (p.Pro678_Thr679insVal) | gnomAD v4 |
7 | g.117592444C>A | CA457449622 | CFTR | c.2277C>A (p.Pro759=) c.*1991C>A (n.*1991C>A) c.2094C>A (p.Pro698=) c.*577C>A (n.*577C>A) c.*2101C>A (n.*2101C>A) c.1851C>A (p.Pro617=) c.1402-10382C>A (n.1402-10382C>A) c.2187C>A (p.Pro729=) c.2367C>A (p.Pro789=) c.2034C>A (p.Pro678=) | |
7 | g.117592444C>G | CA457449624 | CFTR | c.2277C>G (p.Pro759=) c.*1991C>G (n.*1991C>G) c.2094C>G (p.Pro698=) c.*577C>G (n.*577C>G) c.*2101C>G (n.*2101C>G) c.1851C>G (p.Pro617=) c.1402-10382C>G (n.1402-10382C>G) c.2187C>G (p.Pro729=) c.2367C>G (p.Pro789=) c.2034C>G (p.Pro678=) | |
7 | g.117592444C>T | CA457449627 | CFTR | c.2277C>T (p.Pro759=) c.*1991C>T (n.*1991C>T) c.2094C>T (p.Pro698=) c.*577C>T (n.*577C>T) c.*2101C>T (n.*2101C>T) c.1851C>T (p.Pro617=) c.1402-10382C>T (n.1402-10382C>T) c.2187C>T (p.Pro729=) c.2367C>T (p.Pro789=) c.2034C>T (p.Pro678=) | |
7 | g.117592445A>C | CA368980799 | CFTR | c.2278A>C (p.Thr760Pro) c.*1992A>C (n.*1992A>C) c.2095A>C (p.Thr699Pro) c.*578A>C (n.*578A>C) c.*2102A>C (n.*2102A>C) c.1852A>C (p.Thr618Pro) c.1402-10381A>C (n.1402-10381A>C) c.2188A>C (p.Thr730Pro) c.2368A>C (p.Thr790Pro) c.2035A>C (p.Thr679Pro) | |
7 | g.117592445A>G | CA368980795 | CFTR | c.2278A>G (p.Thr760Ala) c.*1992A>G (n.*1992A>G) c.2095A>G (p.Thr699Ala) c.*578A>G (n.*578A>G) c.*2102A>G (n.*2102A>G) c.1852A>G (p.Thr618Ala) c.1402-10381A>G (n.1402-10381A>G) c.2188A>G (p.Thr730Ala) c.2368A>G (p.Thr790Ala) c.2035A>G (p.Thr679Ala) | ClinVar |
7 | g.117592445A>T | CA368980797 | CFTR | c.2278A>T (p.Thr760Ser) c.*1992A>T (n.*1992A>T) c.2095A>T (p.Thr699Ser) c.*578A>T (n.*578A>T) c.*2102A>T (n.*2102A>T) c.1852A>T (p.Thr618Ser) c.1402-10381A>T (n.1402-10381A>T) c.2188A>T (p.Thr730Ser) c.2368A>T (p.Thr790Ser) c.2035A>T (p.Thr679Ser) | ClinVar |
7 | g.117592445dup | CA2573141692 | CFTR | c.2278dup (p.Thr760AsnfsTer19) c.*1992dup (n.*1992dup) c.2095dup (p.Thr699AsnfsTer19) c.*578dup (n.*578dup) c.*2102dup (n.*2102dup) c.1852dup (p.Thr618AsnfsTer19) c.1402-10381dup (n.1402-10381dup) c.2188dup (p.Thr730AsnfsTer19) c.2368dup (p.Thr790AsnfsTer19) c.2035dup (p.Thr679AsnfsTer19) | ClinVar dbSNP |
7 | g.117592446C>A | CA368980803 | CFTR | c.2279C>A (p.Thr760Lys) c.*1993C>A (n.*1993C>A) c.2096C>A (p.Thr699Lys) c.*579C>A (n.*579C>A) c.*2103C>A (n.*2103C>A) c.1853C>A (p.Thr618Lys) c.1402-10380C>A (n.1402-10380C>A) c.2189C>A (p.Thr730Lys) c.2369C>A (p.Thr790Lys) c.2036C>A (p.Thr679Lys) | |
7 | g.117592446C= | CA1737395175 | CFTR | c.2279C= (p.Thr760=) c.*1993C= (n.*1993C=) c.2096C= (p.Thr699=) c.*579C= (n.*579C=) c.*2103C= (n.*2103C=) c.1853C= (p.Thr618=) c.1402-10380C= (n.1402-10380C=) c.2189C= (p.Thr730=) c.2369C= (p.Thr790=) c.2036C= (p.Thr679=) | |
7 | g.117592446C>G | CA4451165 | CFTR | c.2279C>G (p.Thr760Arg) c.*1993C>G (n.*1993C>G) c.2096C>G (p.Thr699Arg) c.*579C>G (n.*579C>G) c.*2103C>G (n.*2103C>G) c.1853C>G (p.Thr618Arg) c.1402-10380C>G (n.1402-10380C>G) c.2189C>G (p.Thr730Arg) c.2369C>G (p.Thr790Arg) c.2036C>G (p.Thr679Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.117592446C>T | CA326786 | CFTR | c.2279C>T (p.Thr760Met) c.*1993C>T (n.*1993C>T) c.2096C>T (p.Thr699Met) c.*579C>T (n.*579C>T) c.*2103C>T (n.*2103C>T) c.1853C>T (p.Thr618Met) c.1402-10380C>T (n.1402-10380C>T) c.2189C>T (p.Thr730Met) c.2369C>T (p.Thr790Met) c.2036C>T (p.Thr679Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.117592447G>A | CA4451166 | CFTR | c.2280G>A (p.Thr760=) c.*1994G>A (n.*1994G>A) c.2097G>A (p.Thr699=) c.*580G>A (n.*580G>A) c.*2104G>A (n.*2104G>A) c.1854G>A (p.Thr618=) c.1402-10379G>A (n.1402-10379G>A) c.2190G>A (p.Thr730=) c.2370G>A (p.Thr790=) c.2037G>A (p.Thr679=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.117592447G>C | CA457449632 | CFTR | c.2280G>C (p.Thr760=) c.*1994G>C (n.*1994G>C) c.2097G>C (p.Thr699=) c.*580G>C (n.*580G>C) c.*2104G>C (n.*2104G>C) c.1854G>C (p.Thr618=) c.1402-10379G>C (n.1402-10379G>C) c.2190G>C (p.Thr730=) c.2370G>C (p.Thr790=) c.2037G>C (p.Thr679=) | gnomAD v4 |
7 | g.117592447G= | CA1737395180 | CFTR | c.2280G= (p.Thr760=) c.*1994G= (n.*1994G=) c.2097G= (p.Thr699=) c.*580G= (n.*580G=) c.*2104G= (n.*2104G=) c.1854G= (p.Thr618=) c.1402-10379G= (n.1402-10379G=) c.2190G= (p.Thr730=) c.2370G= (p.Thr790=) c.2037G= (p.Thr679=) | |
7 | g.117592447G>T | CA457449631 | CFTR | c.2280G>T (p.Thr760=) c.*1994G>T (n.*1994G>T) c.2097G>T (p.Thr699=) c.*580G>T (n.*580G>T) c.*2104G>T (n.*2104G>T) c.1854G>T (p.Thr618=) c.1402-10379G>T (n.1402-10379G>T) c.2190G>T (p.Thr730=) c.2370G>T (p.Thr790=) c.2037G>T (p.Thr679=) | |
7 | g.117592448C>A | CA368980815 | CFTR | c.2281C>A (p.Leu761Ile) c.*1995C>A (n.*1995C>A) c.2098C>A (p.Leu700Ile) c.*581C>A (n.*581C>A) c.*2105C>A (n.*2105C>A) c.1855C>A (p.Leu619Ile) c.1402-10378C>A (n.1402-10378C>A) c.2191C>A (p.Leu731Ile) c.2371C>A (p.Leu791Ile) c.2038C>A (p.Leu680Ile) | ClinVar |
7 | g.117592448C>G | CA368980817 | CFTR | c.2281C>G (p.Leu761Val) c.*1995C>G (n.*1995C>G) c.2098C>G (p.Leu700Val) c.*581C>G (n.*581C>G) c.*2105C>G (n.*2105C>G) c.1855C>G (p.Leu619Val) c.1402-10378C>G (n.1402-10378C>G) c.2191C>G (p.Leu731Val) c.2371C>G (p.Leu791Val) c.2038C>G (p.Leu680Val) | |
7 | g.117592448C>T | CA368980819 | CFTR | c.2281C>T (p.Leu761Phe) c.*1995C>T (n.*1995C>T) c.2098C>T (p.Leu700Phe) c.*581C>T (n.*581C>T) c.*2105C>T (n.*2105C>T) c.1855C>T (p.Leu619Phe) c.1402-10378C>T (n.1402-10378C>T) c.2191C>T (p.Leu731Phe) c.2371C>T (p.Leu791Phe) c.2038C>T (p.Leu680Phe) | gnomAD v4 |
7 | g.117592449T>A | CA368980823 | CFTR | c.2282T>A (p.Leu761His) c.*1996T>A (n.*1996T>A) c.2099T>A (p.Leu700His) c.*582T>A (n.*582T>A) c.*2106T>A (n.*2106T>A) c.1856T>A (p.Leu619His) c.1402-10377T>A (n.1402-10377T>A) c.2192T>A (p.Leu731His) c.2372T>A (p.Leu791His) c.2039T>A (p.Leu680His) | |
7 | g.117592449T>C | CA164948166 | CFTR | c.2282T>C (p.Leu761Pro) c.*1996T>C (n.*1996T>C) c.2099T>C (p.Leu700Pro) c.*582T>C (n.*582T>C) c.*2106T>C (n.*2106T>C) c.1856T>C (p.Leu619Pro) c.1402-10377T>C (n.1402-10377T>C) c.2192T>C (p.Leu731Pro) c.2372T>C (p.Leu791Pro) c.2039T>C (p.Leu680Pro) | dbSNP |
7 | g.117592449T>G | CA368980827 | CFTR | c.2282T>G (p.Leu761Arg) c.*1996T>G (n.*1996T>G) c.2099T>G (p.Leu700Arg) c.*582T>G (n.*582T>G) c.*2106T>G (n.*2106T>G) c.1856T>G (p.Leu619Arg) c.1402-10377T>G (n.1402-10377T>G) c.2192T>G (p.Leu731Arg) c.2372T>G (p.Leu791Arg) c.2039T>G (p.Leu680Arg) | |
7 | g.117592449T= | CA1737395183 | CFTR | c.2282T= (p.Leu761=) c.*1996T= (n.*1996T=) c.2099T= (p.Leu700=) c.*582T= (n.*582T=) c.*2106T= (n.*2106T=) c.1856T= (p.Leu619=) c.1402-10377T= (n.1402-10377T=) c.2192T= (p.Leu731=) c.2372T= (p.Leu791=) c.2039T= (p.Leu680=) | |
7 | g.117592450dup | CA2580076542 | CFTR | c.2283dup (p.Gln762SerfsTer17) c.*1997dup (n.*1997dup) c.2100dup (p.Gln701SerfsTer17) c.*583dup (n.*583dup) c.*2107dup (n.*2107dup) c.1857dup (p.Gln620SerfsTer17) c.1402-10376dup (n.1402-10376dup) c.2193dup (p.Gln732SerfsTer17) c.2373dup (p.Gln792SerfsTer17) c.2040dup (p.Gln681SerfsTer17) | ClinVar |
7 | g.117592450T>A | CA457449638 | CFTR | c.2283T>A (p.Leu761=) c.*1997T>A (n.*1997T>A) c.2100T>A (p.Leu700=) c.*583T>A (n.*583T>A) c.*2107T>A (n.*2107T>A) c.1857T>A (p.Leu619=) c.1402-10376T>A (n.1402-10376T>A) c.2193T>A (p.Leu731=) c.2373T>A (p.Leu791=) c.2040T>A (p.Leu680=) | |
7 | g.117592450T>C | CA457449640 | CFTR | c.2283T>C (p.Leu761=) c.*1997T>C (n.*1997T>C) c.2100T>C (p.Leu700=) c.*583T>C (n.*583T>C) c.*2107T>C (n.*2107T>C) c.1857T>C (p.Leu619=) c.1402-10376T>C (n.1402-10376T>C) c.2193T>C (p.Leu731=) c.2373T>C (p.Leu791=) c.2040T>C (p.Leu680=) | |
7 | g.117592450T>G | CA457449645 | CFTR | c.2283T>G (p.Leu761=) c.*1997T>G (n.*1997T>G) c.2100T>G (p.Leu700=) c.*583T>G (n.*583T>G) c.*2107T>G (n.*2107T>G) c.1857T>G (p.Leu619=) c.1402-10376T>G (n.1402-10376T>G) c.2193T>G (p.Leu731=) c.2373T>G (p.Leu791=) c.2040T>G (p.Leu680=) | ClinVar |
7 | g.117592451C>A | CA368980834 | CFTR | c.2284C>A (p.Gln762Lys) c.*1998C>A (n.*1998C>A) c.2101C>A (p.Gln701Lys) c.*584C>A (n.*584C>A) c.*2108C>A (n.*2108C>A) c.1858C>A (p.Gln620Lys) c.1402-10375C>A (n.1402-10375C>A) c.2194C>A (p.Gln732Lys) c.2374C>A (p.Gln792Lys) c.2041C>A (p.Gln681Lys) | |
7 | g.117592451C>G | CA368980830 | CFTR | c.2284C>G (p.Gln762Glu) c.*1998C>G (n.*1998C>G) c.2101C>G (p.Gln701Glu) c.*584C>G (n.*584C>G) c.*2108C>G (n.*2108C>G) c.1858C>G (p.Gln620Glu) c.1402-10375C>G (n.1402-10375C>G) c.2194C>G (p.Gln732Glu) c.2374C>G (p.Gln792Glu) c.2041C>G (p.Gln681Glu) | |
7 | g.117592451C>T | CA368980832 | CFTR | c.2284C>T (p.Gln762Ter) c.*1998C>T (n.*1998C>T) c.2101C>T (p.Gln701Ter) c.*584C>T (n.*584C>T) c.*2108C>T (n.*2108C>T) c.1858C>T (p.Gln620Ter) c.1402-10375C>T (n.1402-10375C>T) c.2194C>T (p.Gln732Ter) c.2374C>T (p.Gln792Ter) c.2041C>T (p.Gln681Ter) | COSMIC |
7 | g.117592452A>C | CA368980838 | CFTR | c.2285A>C (p.Gln762Pro) c.*1999A>C (n.*1999A>C) c.2102A>C (p.Gln701Pro) c.*585A>C (n.*585A>C) c.*2109A>C (n.*2109A>C) c.1859A>C (p.Gln620Pro) c.1402-10374A>C (n.1402-10374A>C) c.2195A>C (p.Gln732Pro) c.2375A>C (p.Gln792Pro) c.2042A>C (p.Gln681Pro) | |
7 | g.117592452A>G | CA368980840 | CFTR | c.2285A>G (p.Gln762Arg) c.*1999A>G (n.*1999A>G) c.2102A>G (p.Gln701Arg) c.*585A>G (n.*585A>G) c.*2109A>G (n.*2109A>G) c.1859A>G (p.Gln620Arg) c.1402-10374A>G (n.1402-10374A>G) c.2195A>G (p.Gln732Arg) c.2375A>G (p.Gln792Arg) c.2042A>G (p.Gln681Arg) | |
7 | g.117592452A>T | CA368980842 | CFTR | c.2285A>T (p.Gln762Leu) c.*1999A>T (n.*1999A>T) c.2102A>T (p.Gln701Leu) c.*585A>T (n.*585A>T) c.*2109A>T (n.*2109A>T) c.1859A>T (p.Gln620Leu) c.1402-10374A>T (n.1402-10374A>T) c.2195A>T (p.Gln732Leu) c.2375A>T (p.Gln792Leu) c.2042A>T (p.Gln681Leu) | |
7 | g.117592453G>A | CA457449653 | CFTR | c.2286G>A (p.Gln762=) c.*2000G>A (n.*2000G>A) c.2103G>A (p.Gln701=) c.*586G>A (n.*586G>A) c.*2110G>A (n.*2110G>A) c.1860G>A (p.Gln620=) c.1402-10373G>A (n.1402-10373G>A) c.2196G>A (p.Gln732=) c.2376G>A (p.Gln792=) c.2043G>A (p.Gln681=) | ClinVar |
7 | g.117592453G>C | CA368980845 | CFTR | c.2286G>C (p.Gln762His) c.*2000G>C (n.*2000G>C) c.2103G>C (p.Gln701His) c.*586G>C (n.*586G>C) c.*2110G>C (n.*2110G>C) c.1860G>C (p.Gln620His) c.1402-10373G>C (n.1402-10373G>C) c.2196G>C (p.Gln732His) c.2376G>C (p.Gln792His) c.2043G>C (p.Gln681His) | |
7 | g.117592453G= | CA1737395188 | CFTR | c.2286G= (p.Gln762=) c.*2000G= (n.*2000G=) c.2103G= (p.Gln701=) c.*586G= (n.*586G=) c.*2110G= (n.*2110G=) c.1860G= (p.Gln620=) c.1402-10373G= (n.1402-10373G=) c.2196G= (p.Gln732=) c.2376G= (p.Gln792=) c.2043G= (p.Gln681=) | |
7 | g.117592453G>T | CA326788 | CFTR | c.2286G>T (p.Gln762His) c.*2000G>T (n.*2000G>T) c.2103G>T (p.Gln701His) c.*586G>T (n.*586G>T) c.*2110G>T (n.*2110G>T) c.1860G>T (p.Gln620His) c.1402-10373G>T (n.1402-10373G>T) c.2196G>T (p.Gln732His) c.2376G>T (p.Gln792His) c.2043G>T (p.Gln681His) | dbSNP gnomAD v4 |
7 | g.117592454G>A | CA368980850 | CFTR | c.2287G>A (p.Ala763Thr) c.*2001G>A (n.*2001G>A) c.2104G>A (p.Ala702Thr) c.*587G>A (n.*587G>A) c.*2111G>A (n.*2111G>A) c.1861G>A (p.Ala621Thr) c.1402-10372G>A (n.1402-10372G>A) c.2197G>A (p.Ala733Thr) c.2377G>A (p.Ala793Thr) c.2044G>A (p.Ala682Thr) | ClinVar dbSNP gnomAD v4 |
7 | g.117592454G>C | CA368980852 | CFTR | c.2287G>C (p.Ala763Pro) c.*2001G>C (n.*2001G>C) c.2104G>C (p.Ala702Pro) c.*587G>C (n.*587G>C) c.*2111G>C (n.*2111G>C) c.1861G>C (p.Ala621Pro) c.1402-10372G>C (n.1402-10372G>C) c.2197G>C (p.Ala733Pro) c.2377G>C (p.Ala793Pro) c.2044G>C (p.Ala682Pro) | |
7 | g.117592454G>T | CA368980855 | CFTR | c.2287G>T (p.Ala763Ser) c.*2001G>T (n.*2001G>T) c.2104G>T (p.Ala702Ser) c.*587G>T (n.*587G>T) c.*2111G>T (n.*2111G>T) c.1861G>T (p.Ala621Ser) c.1402-10372G>T (n.1402-10372G>T) c.2197G>T (p.Ala733Ser) c.2377G>T (p.Ala793Ser) c.2044G>T (p.Ala682Ser) | ClinVar |
7 | g.117592455C>A | CA368980858 | CFTR | c.2288C>A (p.Ala763Glu) c.*2002C>A (n.*2002C>A) c.2105C>A (p.Ala702Glu) c.*588C>A (n.*588C>A) c.*2112C>A (n.*2112C>A) c.1862C>A (p.Ala621Glu) c.1402-10371C>A (n.1402-10371C>A) c.2198C>A (p.Ala733Glu) c.2378C>A (p.Ala793Glu) c.2045C>A (p.Ala682Glu) | |
7 | g.117592455C>G | CA368980860 | CFTR | c.2288C>G (p.Ala763Gly) c.*2002C>G (n.*2002C>G) c.2105C>G (p.Ala702Gly) c.*588C>G (n.*588C>G) c.*2112C>G (n.*2112C>G) c.1862C>G (p.Ala621Gly) c.1402-10371C>G (n.1402-10371C>G) c.2198C>G (p.Ala733Gly) c.2378C>G (p.Ala793Gly) c.2045C>G (p.Ala682Gly) | ClinVar |
7 | g.117592455C>T | CA368980863 | CFTR | c.2288C>T (p.Ala763Val) c.*2002C>T (n.*2002C>T) c.2105C>T (p.Ala702Val) c.*588C>T (n.*588C>T) c.*2112C>T (n.*2112C>T) c.1862C>T (p.Ala621Val) c.1402-10371C>T (n.1402-10371C>T) c.2198C>T (p.Ala733Val) c.2378C>T (p.Ala793Val) c.2045C>T (p.Ala682Val) | |
7 | g.117592456A= | CA1737395189 | CFTR | c.2289A= (p.Ala763=) c.*2003A= (n.*2003A=) c.2106A= (p.Ala702=) c.*589A= (n.*589A=) c.*2113A= (n.*2113A=) c.1863A= (p.Ala621=) c.1402-10370A= (n.1402-10370A=) c.2199A= (p.Ala733=) c.2379A= (p.Ala793=) c.2046A= (p.Ala682=) | |
7 | g.117592456A>C | CA457449660 | CFTR | c.2289A>C (p.Ala763=) c.*2003A>C (n.*2003A>C) c.2106A>C (p.Ala702=) c.*589A>C (n.*589A>C) c.*2113A>C (n.*2113A>C) c.1863A>C (p.Ala621=) c.1402-10370A>C (n.1402-10370A>C) c.2199A>C (p.Ala733=) c.2379A>C (p.Ala793=) c.2046A>C (p.Ala682=) | |
7 | g.117592456A>G | CA457449661 | CFTR | c.2289A>G (p.Ala763=) c.*2003A>G (n.*2003A>G) c.2106A>G (p.Ala702=) c.*589A>G (n.*589A>G) c.*2113A>G (n.*2113A>G) c.1863A>G (p.Ala621=) c.1402-10370A>G (n.1402-10370A>G) c.2199A>G (p.Ala733=) c.2379A>G (p.Ala793=) c.2046A>G (p.Ala682=) | ClinVar dbSNP |
7 | g.117592456A>T | CA457449663 | CFTR | c.2289A>T (p.Ala763=) c.*2003A>T (n.*2003A>T) c.2106A>T (p.Ala702=) c.*589A>T (n.*589A>T) c.*2113A>T (n.*2113A>T) c.1863A>T (p.Ala621=) c.1402-10370A>T (n.1402-10370A>T) c.2199A>T (p.Ala733=) c.2379A>T (p.Ala793=) c.2046A>T (p.Ala682=) | |
7 | g.117592457C>A | CA457449666 | CFTR | c.2290C>A (p.Arg764=) c.*2004C>A (n.*2004C>A) c.2107C>A (p.Arg703=) c.*590C>A (n.*590C>A) c.*2114C>A (n.*2114C>A) c.1864C>A (p.Arg622=) c.1402-10369C>A (n.1402-10369C>A) c.2200C>A (p.Arg734=) c.2380C>A (p.Arg794=) c.2047C>A (p.Arg683=) | ClinVar gnomAD v4 |
7 | g.117592457C= | CA1737395194 | CFTR | c.2290C= (p.Arg764=) c.*2004C= (n.*2004C=) c.2107C= (p.Arg703=) c.*590C= (n.*590C=) c.*2114C= (n.*2114C=) c.1864C= (p.Arg622=) c.1402-10369C= (n.1402-10369C=) c.2200C= (p.Arg734=) c.2380C= (p.Arg794=) c.2047C= (p.Arg683=) | |
7 | g.117592457C>G | CA368980865 | CFTR | c.2290C>G (p.Arg764Gly) c.*2004C>G (n.*2004C>G) c.2107C>G (p.Arg703Gly) c.*590C>G (n.*590C>G) c.*2114C>G (n.*2114C>G) c.1864C>G (p.Arg622Gly) c.1402-10369C>G (n.1402-10369C>G) c.2200C>G (p.Arg734Gly) c.2380C>G (p.Arg794Gly) c.2047C>G (p.Arg683Gly) | |
7 | g.117592457C>T | CA328100 | CFTR | c.2290C>T (p.Arg764Ter) c.*2004C>T (n.*2004C>T) c.2107C>T (p.Arg703Ter) c.*590C>T (n.*590C>T) c.*2114C>T (n.*2114C>T) c.1864C>T (p.Arg622Ter) c.1402-10369C>T (n.1402-10369C>T) c.2200C>T (p.Arg734Ter) c.2380C>T (p.Arg794Ter) c.2047C>T (p.Arg683Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
7 | g.117592457_117592458delinsCG | CA1737395200 | CFTR | c.2290_2291delinsCG (p.Arg764=) c.*2004_*2005delinsCG (n.*2004_*2005delinsCG) c.2107_2108delinsCG (p.Arg703=) c.*590_*591delinsCG (n.*590_*591delinsCG) c.*2114_*2115delinsCG (n.*2114_*2115delinsCG) c.1864_1865delinsCG (p.Arg622=) c.1402-10369_1402-10368delinsCG (n.1402-10369_1402-10368delinsCG) c.2200_2201delinsCG (p.Arg734=) c.2380_2381delinsCG (p.Arg794=) c.2047_2048delinsCG (p.Arg683=) | |
7 | g.117592458del | CA325606 | CFTR | c.2291del (p.Arg764GlnfsTer7) c.*2005del (n.*2005del) c.2108del (p.Arg703GlnfsTer7) c.*591del (n.*591del) c.*2115del (n.*2115del) c.1865del (p.Arg622GlnfsTer7) c.1402-10368del (n.1402-10368del) c.2201del (p.Arg734GlnfsTer7) c.2381del (p.Arg794GlnfsTer7) c.2048del (p.Arg683GlnfsTer7) | ClinVar dbSNP |
7 | g.117592458G>A | CA368980869 | CFTR | c.2291G>A (p.Arg764Gln) c.*2005G>A (n.*2005G>A) c.2108G>A (p.Arg703Gln) c.*591G>A (n.*591G>A) c.*2115G>A (n.*2115G>A) c.1865G>A (p.Arg622Gln) c.1402-10368G>A (n.1402-10368G>A) c.2201G>A (p.Arg734Gln) c.2381G>A (p.Arg794Gln) c.2048G>A (p.Arg683Gln) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
7 | g.117592458G>C | CA368980871 | CFTR | c.2291G>C (p.Arg764Pro) c.*2005G>C (n.*2005G>C) c.2108G>C (p.Arg703Pro) c.*591G>C (n.*591G>C) c.*2115G>C (n.*2115G>C) c.1865G>C (p.Arg622Pro) c.1402-10368G>C (n.1402-10368G>C) c.2201G>C (p.Arg734Pro) c.2381G>C (p.Arg794Pro) c.2048G>C (p.Arg683Pro) | |
7 | g.117592458G= | CA1737395210 | CFTR | c.2291G= (p.Arg764=) c.*2005G= (n.*2005G=) c.2108G= (p.Arg703=) c.*591G= (n.*591G=) c.*2115G= (n.*2115G=) c.1865G= (p.Arg622=) c.1402-10368G= (n.1402-10368G=) c.2201G= (p.Arg734=) c.2381G= (p.Arg794=) c.2048G= (p.Arg683=) | |
7 | g.117592458G>T | CA368980873 | CFTR | c.2291G>T (p.Arg764Leu) c.*2005G>T (n.*2005G>T) c.2108G>T (p.Arg703Leu) c.*591G>T (n.*591G>T) c.*2115G>T (n.*2115G>T) c.1865G>T (p.Arg622Leu) c.1402-10368G>T (n.1402-10368G>T) c.2201G>T (p.Arg734Leu) c.2381G>T (p.Arg794Leu) c.2048G>T (p.Arg683Leu) | |
7 | g.117592459A>C | CA457449669 | CFTR | c.2292A>C (p.Arg764=) c.*2006A>C (n.*2006A>C) c.2109A>C (p.Arg703=) c.*592A>C (n.*592A>C) c.*2116A>C (n.*2116A>C) c.1866A>C (p.Arg622=) c.1402-10367A>C (n.1402-10367A>C) c.2202A>C (p.Arg734=) c.2382A>C (p.Arg794=) c.2049A>C (p.Arg683=) | |
7 | g.117592459A>G | CA457449670 | CFTR | c.2292A>G (p.Arg764=) c.*2006A>G (n.*2006A>G) c.2109A>G (p.Arg703=) c.*592A>G (n.*592A>G) c.*2116A>G (n.*2116A>G) c.1866A>G (p.Arg622=) c.1402-10367A>G (n.1402-10367A>G) c.2202A>G (p.Arg734=) c.2382A>G (p.Arg794=) c.2049A>G (p.Arg683=) | gnomAD v4 |
7 | g.117592459A>T | CA457449671 | CFTR | c.2292A>T (p.Arg764=) c.*2006A>T (n.*2006A>T) c.2109A>T (p.Arg703=) c.*592A>T (n.*592A>T) c.*2116A>T (n.*2116A>T) c.1866A>T (p.Arg622=) c.1402-10367A>T (n.1402-10367A>T) c.2202A>T (p.Arg734=) c.2382A>T (p.Arg794=) c.2049A>T (p.Arg683=) | |
7 | g.117592460A>C | CA457449673 | CFTR | c.2293A>C (p.Arg765=) c.*2007A>C (n.*2007A>C) c.2110A>C (p.Arg704=) c.*593A>C (n.*593A>C) c.*2117A>C (n.*2117A>C) c.1867A>C (p.Arg623=) c.1402-10366A>C (n.1402-10366A>C) c.2203A>C (p.Arg735=) c.2383A>C (p.Arg795=) c.2050A>C (p.Arg684=) | |
7 | g.117592460A>G | CA368980876 | CFTR | c.2293A>G (p.Arg765Gly) c.*2007A>G (n.*2007A>G) c.2110A>G (p.Arg704Gly) c.*593A>G (n.*593A>G) c.*2117A>G (n.*2117A>G) c.1867A>G (p.Arg623Gly) c.1402-10366A>G (n.1402-10366A>G) c.2203A>G (p.Arg735Gly) c.2383A>G (p.Arg795Gly) c.2050A>G (p.Arg684Gly) | ClinVar |
7 | g.117592460A>T | CA368980878 | CFTR | c.2293A>T (p.Arg765Trp) c.*2007A>T (n.*2007A>T) c.2110A>T (p.Arg704Trp) c.*593A>T (n.*593A>T) c.*2117A>T (n.*2117A>T) c.1867A>T (p.Arg623Trp) c.1402-10366A>T (n.1402-10366A>T) c.2203A>T (p.Arg735Trp) c.2383A>T (p.Arg795Trp) c.2050A>T (p.Arg684Trp) | |
7 | g.117592461G>A | CA4451167 | CFTR | c.2294G>A (p.Arg765Lys) c.*2008G>A (n.*2008G>A) c.2111G>A (p.Arg704Lys) c.*594G>A (n.*594G>A) c.*2118G>A (n.*2118G>A) c.1868G>A (p.Arg623Lys) c.1402-10365G>A (n.1402-10365G>A) c.2204G>A (p.Arg735Lys) c.2384G>A (p.Arg795Lys) c.2051G>A (p.Arg684Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.117592461G>C | CA368980882 | CFTR | c.2294G>C (p.Arg765Thr) c.*2008G>C (n.*2008G>C) c.2111G>C (p.Arg704Thr) c.*594G>C (n.*594G>C) c.*2118G>C (n.*2118G>C) c.1868G>C (p.Arg623Thr) c.1402-10365G>C (n.1402-10365G>C) c.2204G>C (p.Arg735Thr) c.2384G>C (p.Arg795Thr) c.2051G>C (p.Arg684Thr) | |
7 | g.117592461G= | CA1737395219 | CFTR | c.2294G= (p.Arg765=) c.*2008G= (n.*2008G=) c.2111G= (p.Arg704=) c.*594G= (n.*594G=) c.*2118G= (n.*2118G=) c.1868G= (p.Arg623=) c.1402-10365G= (n.1402-10365G=) c.2204G= (p.Arg735=) c.2384G= (p.Arg795=) c.2051G= (p.Arg684=) | |
7 | g.117592461G>T | CA368980884 | CFTR | c.2294G>T (p.Arg765Met) c.*2008G>T (n.*2008G>T) c.2111G>T (p.Arg704Met) c.*594G>T (n.*594G>T) c.*2118G>T (n.*2118G>T) c.1868G>T (p.Arg623Met) c.1402-10365G>T (n.1402-10365G>T) c.2204G>T (p.Arg735Met) c.2384G>T (p.Arg795Met) c.2051G>T (p.Arg684Met) | |
7 | g.117592462G>A | CA457449676 | CFTR | c.2295G>A (p.Arg765=) c.*2009G>A (n.*2009G>A) c.2112G>A (p.Arg704=) c.*595G>A (n.*595G>A) c.*2119G>A (n.*2119G>A) c.1869G>A (p.Arg623=) c.1402-10364G>A (n.1402-10364G>A) c.2205G>A (p.Arg735=) c.2385G>A (p.Arg795=) c.2052G>A (p.Arg684=) | ClinVar |
7 | g.117592462G>C | CA368980887 | CFTR | c.2295G>C (p.Arg765Ser) c.*2009G>C (n.*2009G>C) c.2112G>C (p.Arg704Ser) c.*595G>C (n.*595G>C) c.*2119G>C (n.*2119G>C) c.1869G>C (p.Arg623Ser) c.1402-10364G>C (n.1402-10364G>C) c.2205G>C (p.Arg735Ser) c.2385G>C (p.Arg795Ser) c.2052G>C (p.Arg684Ser) | |
7 | g.117592462G>T | CA368980888 | CFTR | c.2295G>T (p.Arg765Ser) c.*2009G>T (n.*2009G>T) c.2112G>T (p.Arg704Ser) c.*595G>T (n.*595G>T) c.*2119G>T (n.*2119G>T) c.1869G>T (p.Arg623Ser) c.1402-10364G>T (n.1402-10364G>T) c.2205G>T (p.Arg735Ser) c.2385G>T (p.Arg795Ser) c.2052G>T (p.Arg684Ser) | gnomAD v4 |
7 | g.117592463A>C | CA457449680 | CFTR | c.2296A>C (p.Arg766=) c.*2010A>C (n.*2010A>C) c.2113A>C (p.Arg705=) c.*596A>C (n.*596A>C) c.*2120A>C (n.*2120A>C) c.1870A>C (p.Arg624=) c.1402-10363A>C (n.1402-10363A>C) c.2206A>C (p.Arg736=) c.2386A>C (p.Arg796=) c.2053A>C (p.Arg685=) | |
7 | g.117592463A>G | CA368980892 | CFTR | c.2296A>G (p.Arg766Gly) c.*2010A>G (n.*2010A>G) c.2113A>G (p.Arg705Gly) c.*596A>G (n.*596A>G) c.*2120A>G (n.*2120A>G) c.1870A>G (p.Arg624Gly) c.1402-10363A>G (n.1402-10363A>G) c.2206A>G (p.Arg736Gly) c.2386A>G (p.Arg796Gly) c.2053A>G (p.Arg685Gly) | |
7 | g.117592463A>T | CA368980894 | CFTR | c.2296A>T (p.Arg766Trp) c.*2010A>T (n.*2010A>T) c.2113A>T (p.Arg705Trp) c.*596A>T (n.*596A>T) c.*2120A>T (n.*2120A>T) c.1870A>T (p.Arg624Trp) c.1402-10363A>T (n.1402-10363A>T) c.2206A>T (p.Arg736Trp) c.2386A>T (p.Arg796Trp) c.2053A>T (p.Arg685Trp) | |
7 | g.117592464G>A | CA4451168 | CFTR | c.2297G>A (p.Arg766Lys) c.*2011G>A (n.*2011G>A) c.2114G>A (p.Arg705Lys) c.*597G>A (n.*597G>A) c.*2121G>A (n.*2121G>A) c.1871G>A (p.Arg624Lys) c.1402-10362G>A (n.1402-10362G>A) c.2207G>A (p.Arg736Lys) c.2387G>A (p.Arg796Lys) c.2054G>A (p.Arg685Lys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.117592464G>C | CA368980900 | CFTR | c.2297G>C (p.Arg766Thr) c.*2011G>C (n.*2011G>C) c.2114G>C (p.Arg705Thr) c.*597G>C (n.*597G>C) c.*2121G>C (n.*2121G>C) c.1871G>C (p.Arg624Thr) c.1402-10362G>C (n.1402-10362G>C) c.2207G>C (p.Arg736Thr) c.2387G>C (p.Arg796Thr) c.2054G>C (p.Arg685Thr) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
7 | g.117592464G= | CA1737395223 | CFTR | c.2297G= (p.Arg766=) c.*2011G= (n.*2011G=) c.2114G= (p.Arg705=) c.*597G= (n.*597G=) c.*2121G= (n.*2121G=) c.1871G= (p.Arg624=) c.1402-10362G= (n.1402-10362G=) c.2207G= (p.Arg736=) c.2387G= (p.Arg796=) c.2054G= (p.Arg685=) | |
7 | g.117592464G>T | CA326790 | CFTR | c.2297G>T (p.Arg766Met) c.*2011G>T (n.*2011G>T) c.2114G>T (p.Arg705Met) c.*597G>T (n.*597G>T) c.*2121G>T (n.*2121G>T) c.1871G>T (p.Arg624Met) c.1402-10362G>T (n.1402-10362G>T) c.2207G>T (p.Arg736Met) c.2387G>T (p.Arg796Met) c.2054G>T (p.Arg685Met) | ClinVar dbSNP |
7 | g.117592465G>A | CA457449683 | CFTR | c.2298G>A (p.Arg766=) c.*2012G>A (n.*2012G>A) c.2115G>A (p.Arg705=) c.*598G>A (n.*598G>A) c.*2122G>A (n.*2122G>A) c.1872G>A (p.Arg624=) c.1402-10361G>A (n.1402-10361G>A) c.2208G>A (p.Arg736=) c.2388G>A (p.Arg796=) c.2055G>A (p.Arg685=) | ClinVar |
7 | g.117592465G>C | CA368980903 | CFTR | c.2298G>C (p.Arg766Ser) c.*2012G>C (n.*2012G>C) c.2115G>C (p.Arg705Ser) c.*598G>C (n.*598G>C) c.*2122G>C (n.*2122G>C) c.1872G>C (p.Arg624Ser) c.1402-10361G>C (n.1402-10361G>C) c.2208G>C (p.Arg736Ser) c.2388G>C (p.Arg796Ser) c.2055G>C (p.Arg685Ser) | |
7 | g.117592465G>T | CA368980905 | CFTR | c.2298G>T (p.Arg766Ser) c.*2012G>T (n.*2012G>T) c.2115G>T (p.Arg705Ser) c.*598G>T (n.*598G>T) c.*2122G>T (n.*2122G>T) c.1872G>T (p.Arg624Ser) c.1402-10361G>T (n.1402-10361G>T) c.2208G>T (p.Arg736Ser) c.2388G>T (p.Arg796Ser) c.2055G>T (p.Arg685Ser) | |
7 | g.117592466C>A | CA368980906 | CFTR | c.2299C>A (p.Gln767Lys) c.*2013C>A (n.*2013C>A) c.2116C>A (p.Gln706Lys) c.*599C>A (n.*599C>A) c.*2123C>A (n.*2123C>A) c.1873C>A (p.Gln625Lys) c.1402-10360C>A (n.1402-10360C>A) c.2209C>A (p.Gln737Lys) c.2389C>A (p.Gln797Lys) c.2056C>A (p.Gln686Lys) | |
7 | g.117592466C= | CA1737395230 | CFTR | c.2299C= (p.Gln767=) c.*2013C= (n.*2013C=) c.2116C= (p.Gln706=) c.*599C= (n.*599C=) c.*2123C= (n.*2123C=) c.1873C= (p.Gln625=) c.1402-10360C= (n.1402-10360C=) c.2209C= (p.Gln737=) c.2389C= (p.Gln797=) c.2056C= (p.Gln686=) | |
7 | g.117592466C>G | CA368980909 | CFTR | c.2299C>G (p.Gln767Glu) c.*2013C>G (n.*2013C>G) c.2116C>G (p.Gln706Glu) c.*599C>G (n.*599C>G) c.*2123C>G (n.*2123C>G) c.1873C>G (p.Gln625Glu) c.1402-10360C>G (n.1402-10360C>G) c.2209C>G (p.Gln737Glu) c.2389C>G (p.Gln797Glu) c.2056C>G (p.Gln686Glu) | |
7 | g.117592466C>T | CA368980912 | CFTR | c.2299C>T (p.Gln767Ter) c.*2013C>T (n.*2013C>T) c.2116C>T (p.Gln706Ter) c.*599C>T (n.*599C>T) c.*2123C>T (n.*2123C>T) c.1873C>T (p.Gln625Ter) c.1402-10360C>T (n.1402-10360C>T) c.2209C>T (p.Gln737Ter) c.2389C>T (p.Gln797Ter) c.2056C>T (p.Gln686Ter) | ClinVar dbSNP |
7 | g.117592466_117592467insGACT | CA2684619362 | CFTR | c.2299_2300insGACT (p.Gln767ArgfsTer13) c.*2013_*2014insGACT (n.*2013_*2014insGACT) c.2116_2117insGACT (p.Gln706ArgfsTer13) c.*599_*600insGACT (n.*599_*600insGACT) c.*2123_*2124insGACT (n.*2123_*2124insGACT) c.1873_1874insGACT (p.Gln625ArgfsTer13) c.1402-10360_1402-10359insGACT (n.1402-10360_1402-10359insGACT) c.2209_2210insGACT (p.Gln737ArgfsTer13) c.2389_2390insGACT (p.Gln797ArgfsTer13) c.2056_2057insGACT (p.Gln686ArgfsTer13) | gnomAD v4 |
7 | g.117592467A>C | CA368980914 | CFTR | c.2300A>C (p.Gln767Pro) c.*2014A>C (n.*2014A>C) c.2117A>C (p.Gln706Pro) c.*600A>C (n.*600A>C) c.*2124A>C (n.*2124A>C) c.1874A>C (p.Gln625Pro) c.1402-10359A>C (n.1402-10359A>C) c.2210A>C (p.Gln737Pro) c.2390A>C (p.Gln797Pro) c.2057A>C (p.Gln686Pro) | |
7 | g.117592467A>G | CA368980916 | CFTR | c.2300A>G (p.Gln767Arg) c.*2014A>G (n.*2014A>G) c.2117A>G (p.Gln706Arg) c.*600A>G (n.*600A>G) c.*2124A>G (n.*2124A>G) c.1874A>G (p.Gln625Arg) c.1402-10359A>G (n.1402-10359A>G) c.2210A>G (p.Gln737Arg) c.2390A>G (p.Gln797Arg) c.2057A>G (p.Gln686Arg) | |
7 | g.117592467A>T | CA368980918 | CFTR | c.2300A>T (p.Gln767Leu) c.*2014A>T (n.*2014A>T) c.2117A>T (p.Gln706Leu) c.*600A>T (n.*600A>T) c.*2124A>T (n.*2124A>T) c.1874A>T (p.Gln625Leu) c.1402-10359A>T (n.1402-10359A>T) c.2210A>T (p.Gln737Leu) c.2390A>T (p.Gln797Leu) c.2057A>T (p.Gln686Leu) | gnomAD v4 |
7 | g.117592468del | CA2573141693 | CFTR | c.2301del (p.Gln767HisfsTer4) c.*2015del (n.*2015del) c.2118del (p.Gln706HisfsTer4) c.*601del (n.*601del) c.*2125del (n.*2125del) c.1875del (p.Gln625HisfsTer4) c.1402-10358del (n.1402-10358del) c.2211del (p.Gln737HisfsTer4) c.2391del (p.Gln797HisfsTer4) c.2058del (p.Gln686HisfsTer4) | ClinVar dbSNP |
7 | g.117592468G>A | CA457449689 | CFTR | c.2301G>A (p.Gln767=) c.*2015G>A (n.*2015G>A) c.2118G>A (p.Gln706=) c.*601G>A (n.*601G>A) c.*2125G>A (n.*2125G>A) c.1875G>A (p.Gln625=) c.1402-10358G>A (n.1402-10358G>A) c.2211G>A (p.Gln737=) c.2391G>A (p.Gln797=) c.2058G>A (p.Gln686=) | ClinVar dbSNP |
7 | g.117592468G>C | CA368980921 | CFTR | c.2301G>C (p.Gln767His) c.*2015G>C (n.*2015G>C) c.2118G>C (p.Gln706His) c.*601G>C (n.*601G>C) c.*2125G>C (n.*2125G>C) c.1875G>C (p.Gln625His) c.1402-10358G>C (n.1402-10358G>C) c.2211G>C (p.Gln737His) c.2391G>C (p.Gln797His) c.2058G>C (p.Gln686His) | dbSNP gnomAD v2 |
7 | g.117592468G= | CA1737395236 | CFTR | c.2301G= (p.Gln767=) c.*2015G= (n.*2015G=) c.2118G= (p.Gln706=) c.*601G= (n.*601G=) c.*2125G= (n.*2125G=) c.1875G= (p.Gln625=) c.1402-10358G= (n.1402-10358G=) c.2211G= (p.Gln737=) c.2391G= (p.Gln797=) c.2058G= (p.Gln686=) | |
7 | g.117592468G>T | CA368980923 | CFTR | c.2301G>T (p.Gln767His) c.*2015G>T (n.*2015G>T) c.2118G>T (p.Gln706His) c.*601G>T (n.*601G>T) c.*2125G>T (n.*2125G>T) c.1875G>T (p.Gln625His) c.1402-10358G>T (n.1402-10358G>T) c.2211G>T (p.Gln737His) c.2391G>T (p.Gln797His) c.2058G>T (p.Gln686His) | |
7 | g.117592469T>A | CA368980929 | CFTR | c.2302T>A (p.Ser768Thr) c.*2016T>A (n.*2016T>A) c.2119T>A (p.Ser707Thr) c.*602T>A (n.*602T>A) c.*2126T>A (n.*2126T>A) c.1876T>A (p.Ser626Thr) c.1402-10357T>A (n.1402-10357T>A) c.2212T>A (p.Ser738Thr) c.2392T>A (p.Ser798Thr) c.2059T>A (p.Ser687Thr) | gnomAD v4 |
7 | g.117592469T>C | CA368980931 | CFTR | c.2302T>C (p.Ser768Pro) c.*2016T>C (n.*2016T>C) c.2119T>C (p.Ser707Pro) c.*602T>C (n.*602T>C) c.*2126T>C (n.*2126T>C) c.1876T>C (p.Ser626Pro) c.1402-10357T>C (n.1402-10357T>C) c.2212T>C (p.Ser738Pro) c.2392T>C (p.Ser798Pro) c.2059T>C (p.Ser687Pro) | |
7 | g.117592469T>G | CA368980927 | CFTR | c.2302T>G (p.Ser768Ala) c.*2016T>G (n.*2016T>G) c.2119T>G (p.Ser707Ala) c.*602T>G (n.*602T>G) c.*2126T>G (n.*2126T>G) c.1876T>G (p.Ser626Ala) c.1402-10357T>G (n.1402-10357T>G) c.2212T>G (p.Ser738Ala) c.2392T>G (p.Ser798Ala) c.2059T>G (p.Ser687Ala) | |
7 | g.117592470C>A | CA368980935 | CFTR | c.2303C>A (p.Ser768Tyr) c.*2017C>A (n.*2017C>A) c.2120C>A (p.Ser707Tyr) c.*603C>A (n.*603C>A) c.*2127C>A (n.*2127C>A) c.1877C>A (p.Ser626Tyr) c.1402-10356C>A (n.1402-10356C>A) c.2213C>A (p.Ser738Tyr) c.2393C>A (p.Ser798Tyr) c.2060C>A (p.Ser687Tyr) | |
7 | g.117592470C= | CA1737395241 | CFTR | c.2303C= (p.Ser768=) c.*2017C= (n.*2017C=) c.2120C= (p.Ser707=) c.*603C= (n.*603C=) c.*2127C= (n.*2127C=) c.1877C= (p.Ser626=) c.1402-10356C= (n.1402-10356C=) c.2213C= (p.Ser738=) c.2393C= (p.Ser798=) c.2060C= (p.Ser687=) | |
7 | g.117592470C>G | CA368980933 | CFTR | c.2303C>G (p.Ser768Cys) c.*2017C>G (n.*2017C>G) c.2120C>G (p.Ser707Cys) c.*603C>G (n.*603C>G) c.*2127C>G (n.*2127C>G) c.1877C>G (p.Ser626Cys) c.1402-10356C>G (n.1402-10356C>G) c.2213C>G (p.Ser738Cys) c.2393C>G (p.Ser798Cys) c.2060C>G (p.Ser687Cys) | |
7 | g.117592470C>T | CA368980934 | CFTR | c.2303C>T (p.Ser768Phe) c.*2017C>T (n.*2017C>T) c.2120C>T (p.Ser707Phe) c.*603C>T (n.*603C>T) c.*2127C>T (n.*2127C>T) c.1877C>T (p.Ser626Phe) c.1402-10356C>T (n.1402-10356C>T) c.2213C>T (p.Ser738Phe) c.2393C>T (p.Ser798Phe) c.2060C>T (p.Ser687Phe) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.117592471T>A | CA457449696 | CFTR | c.2304T>A (p.Ser768=) c.*2018T>A (n.*2018T>A) c.2121T>A (p.Ser707=) c.*604T>A (n.*604T>A) c.*2128T>A (n.*2128T>A) c.1878T>A (p.Ser626=) c.1402-10355T>A (n.1402-10355T>A) c.2214T>A (p.Ser738=) c.2394T>A (p.Ser798=) c.2061T>A (p.Ser687=) | ClinVar |
7 | g.117592471T>C | CA457449692 | CFTR | c.2304T>C (p.Ser768=) c.*2018T>C (n.*2018T>C) c.2121T>C (p.Ser707=) c.*604T>C (n.*604T>C) c.*2128T>C (n.*2128T>C) c.1878T>C (p.Ser626=) c.1402-10355T>C (n.1402-10355T>C) c.2214T>C (p.Ser738=) c.2394T>C (p.Ser798=) c.2061T>C (p.Ser687=) | gnomAD v4 |
7 | g.117592471T>G | CA457449695 | CFTR | c.2304T>G (p.Ser768=) c.*2018T>G (n.*2018T>G) c.2121T>G (p.Ser707=) c.*604T>G (n.*604T>G) c.*2128T>G (n.*2128T>G) c.1878T>G (p.Ser626=) c.1402-10355T>G (n.1402-10355T>G) c.2214T>G (p.Ser738=) c.2394T>G (p.Ser798=) c.2061T>G (p.Ser687=) | |
7 | g.117592472G>A | CA368980936 | CFTR | c.2305G>A (p.Val769Ile) c.*2019G>A (n.*2019G>A) c.2122G>A (p.Val708Ile) c.*605G>A (n.*605G>A) c.*2129G>A (n.*2129G>A) c.1879G>A (p.Val627Ile) c.1402-10354G>A (n.1402-10354G>A) c.2215G>A (p.Val739Ile) c.2395G>A (p.Val799Ile) c.2062G>A (p.Val688Ile) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.117592472G>C | CA368980937 | CFTR | c.2305G>C (p.Val769Leu) c.*2019G>C (n.*2019G>C) c.2122G>C (p.Val708Leu) c.*605G>C (n.*605G>C) c.*2129G>C (n.*2129G>C) c.1879G>C (p.Val627Leu) c.1402-10354G>C (n.1402-10354G>C) c.2215G>C (p.Val739Leu) c.2395G>C (p.Val799Leu) c.2062G>C (p.Val688Leu) | |
7 | g.117592472G= | CA1737395247 | CFTR | c.2305G= (p.Val769=) c.*2019G= (n.*2019G=) c.2122G= (p.Val708=) c.*605G= (n.*605G=) c.*2129G= (n.*2129G=) c.1879G= (p.Val627=) c.1402-10354G= (n.1402-10354G=) c.2215G= (p.Val739=) c.2395G= (p.Val799=) c.2062G= (p.Val688=) | |
7 | g.117592472G>T | CA368980938 | CFTR | c.2305G>T (p.Val769Phe) c.*2019G>T (n.*2019G>T) c.2122G>T (p.Val708Phe) c.*605G>T (n.*605G>T) c.*2129G>T (n.*2129G>T) c.1879G>T (p.Val627Phe) c.1402-10354G>T (n.1402-10354G>T) c.2215G>T (p.Val739Phe) c.2395G>T (p.Val799Phe) c.2062G>T (p.Val688Phe) | |
7 | g.117592473T>A | CA368980939 | CFTR | c.2306T>A (p.Val769Asp) c.*2020T>A (n.*2020T>A) c.2123T>A (p.Val708Asp) c.*606T>A (n.*606T>A) c.*2130T>A (n.*2130T>A) c.1880T>A (p.Val627Asp) c.1402-10353T>A (n.1402-10353T>A) c.2216T>A (p.Val739Asp) c.2396T>A (p.Val799Asp) c.2063T>A (p.Val688Asp) | |
7 | g.117592473T>C | CA368980940 | CFTR | c.2306T>C (p.Val769Ala) c.*2020T>C (n.*2020T>C) c.2123T>C (p.Val708Ala) c.*606T>C (n.*606T>C) c.*2130T>C (n.*2130T>C) c.1880T>C (p.Val627Ala) c.1402-10353T>C (n.1402-10353T>C) c.2216T>C (p.Val739Ala) c.2396T>C (p.Val799Ala) c.2063T>C (p.Val688Ala) | |
7 | g.117592473T>G | CA368980941 | CFTR | c.2306T>G (p.Val769Gly) c.*2020T>G (n.*2020T>G) c.2123T>G (p.Val708Gly) c.*606T>G (n.*606T>G) c.*2130T>G (n.*2130T>G) c.1880T>G (p.Val627Gly) c.1402-10353T>G (n.1402-10353T>G) c.2216T>G (p.Val739Gly) c.2396T>G (p.Val799Gly) c.2063T>G (p.Val688Gly) | |
7 | g.117592474C>A | CA457449701 | CFTR | c.2307C>A (p.Val769=) c.*2021C>A (n.*2021C>A) c.2124C>A (p.Val708=) c.*607C>A (n.*607C>A) c.*2131C>A (n.*2131C>A) c.1881C>A (p.Val627=) c.1402-10352C>A (n.1402-10352C>A) c.2217C>A (p.Val739=) c.2397C>A (p.Val799=) c.2064C>A (p.Val688=) | gnomAD v4 |
7 | g.117592474C= | CA1737395249 | CFTR | c.2307C= (p.Val769=) c.*2021C= (n.*2021C=) c.2124C= (p.Val708=) c.*607C= (n.*607C=) c.*2131C= (n.*2131C=) c.1881C= (p.Val627=) c.1402-10352C= (n.1402-10352C=) c.2217C= (p.Val739=) c.2397C= (p.Val799=) c.2064C= (p.Val688=) | |
7 | g.117592474C>G | CA457449705 | CFTR | c.2307C>G (p.Val769=) c.*2021C>G (n.*2021C>G) c.2124C>G (p.Val708=) c.*607C>G (n.*607C>G) c.*2131C>G (n.*2131C>G) c.1881C>G (p.Val627=) c.1402-10352C>G (n.1402-10352C>G) c.2217C>G (p.Val739=) c.2397C>G (p.Val799=) c.2064C>G (p.Val688=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
7 | g.117592474C>T | CA457449703 | CFTR | c.2307C>T (p.Val769=) c.*2021C>T (n.*2021C>T) c.2124C>T (p.Val708=) c.*607C>T (n.*607C>T) c.*2131C>T (n.*2131C>T) c.1881C>T (p.Val627=) c.1402-10352C>T (n.1402-10352C>T) c.2217C>T (p.Val739=) c.2397C>T (p.Val799=) c.2064C>T (p.Val688=) | dbSNP |
7 | g.117592475C>A | CA368980942 | CFTR | c.2308C>A (p.Leu770Met) c.*2022C>A (n.*2022C>A) c.2125C>A (p.Leu709Met) c.*608C>A (n.*608C>A) c.*2132C>A (n.*2132C>A) c.1882C>A (p.Leu628Met) c.1402-10351C>A (n.1402-10351C>A) c.2218C>A (p.Leu740Met) c.2398C>A (p.Leu800Met) c.2065C>A (p.Leu689Met) | |
7 | g.117592475C>G | CA368980943 | CFTR | c.2308C>G (p.Leu770Val) c.*2022C>G (n.*2022C>G) c.2125C>G (p.Leu709Val) c.*608C>G (n.*608C>G) c.*2132C>G (n.*2132C>G) c.1882C>G (p.Leu628Val) c.1402-10351C>G (n.1402-10351C>G) c.2218C>G (p.Leu740Val) c.2398C>G (p.Leu800Val) c.2065C>G (p.Leu689Val) | |
7 | g.117592475C>T | CA457449709 | CFTR | c.2308C>T (p.Leu770=) c.*2022C>T (n.*2022C>T) c.2125C>T (p.Leu709=) c.*608C>T (n.*608C>T) c.*2132C>T (n.*2132C>T) c.1882C>T (p.Leu628=) c.1402-10351C>T (n.1402-10351C>T) c.2218C>T (p.Leu740=) c.2398C>T (p.Leu800=) c.2065C>T (p.Leu689=) | |
7 | g.117592476T>A | CA368980944 | CFTR | c.2309T>A (p.Leu770Gln) c.*2023T>A (n.*2023T>A) c.2126T>A (p.Leu709Gln) c.*609T>A (n.*609T>A) c.*2133T>A (n.*2133T>A) c.1883T>A (p.Leu628Gln) c.1402-10350T>A (n.1402-10350T>A) c.2219T>A (p.Leu740Gln) c.2399T>A (p.Leu800Gln) c.2066T>A (p.Leu689Gln) | |
7 | g.117592476T>C | CA368980945 | CFTR | c.2309T>C (p.Leu770Pro) c.*2023T>C (n.*2023T>C) c.2126T>C (p.Leu709Pro) c.*609T>C (n.*609T>C) c.*2133T>C (n.*2133T>C) c.1883T>C (p.Leu628Pro) c.1402-10350T>C (n.1402-10350T>C) c.2219T>C (p.Leu740Pro) c.2399T>C (p.Leu800Pro) c.2066T>C (p.Leu689Pro) | |
7 | g.117592476T>G | CA368980946 | CFTR | c.2309T>G (p.Leu770Arg) c.*2023T>G (n.*2023T>G) c.2126T>G (p.Leu709Arg) c.*609T>G (n.*609T>G) c.*2133T>G (n.*2133T>G) c.1883T>G (p.Leu628Arg) c.1402-10350T>G (n.1402-10350T>G) c.2219T>G (p.Leu740Arg) c.2399T>G (p.Leu800Arg) c.2066T>G (p.Leu689Arg) | |
7 | g.117592477G>A | CA457449710 | CFTR | c.2310G>A (p.Leu770=) c.*2024G>A (n.*2024G>A) c.2127G>A (p.Leu709=) c.*610G>A (n.*610G>A) c.*2134G>A (n.*2134G>A) c.1884G>A (p.Leu628=) c.1402-10349G>A (n.1402-10349G>A) c.2220G>A (p.Leu740=) c.2400G>A (p.Leu800=) c.2067G>A (p.Leu689=) | |
7 | g.117592477G>C | CA457449712 | CFTR | c.2310G>C (p.Leu770=) c.*2024G>C (n.*2024G>C) c.2127G>C (p.Leu709=) c.*610G>C (n.*610G>C) c.*2134G>C (n.*2134G>C) c.1884G>C (p.Leu628=) c.1402-10349G>C (n.1402-10349G>C) c.2220G>C (p.Leu740=) c.2400G>C (p.Leu800=) c.2067G>C (p.Leu689=) | |
7 | g.117592477G>T | CA457449715 | CFTR | c.2310G>T (p.Leu770=) c.*2024G>T (n.*2024G>T) c.2127G>T (p.Leu709=) c.*610G>T (n.*610G>T) c.*2134G>T (n.*2134G>T) c.1884G>T (p.Leu628=) c.1402-10349G>T (n.1402-10349G>T) c.2220G>T (p.Leu740=) c.2400G>T (p.Leu800=) c.2067G>T (p.Leu689=) | ClinVar |
7 | g.117592478A>C | CA368980949 | CFTR | c.2311A>C (p.Asn771His) c.*2025A>C (n.*2025A>C) c.2128A>C (p.Asn710His) c.*611A>C (n.*611A>C) c.*2135A>C (n.*2135A>C) c.1885A>C (p.Asn629His) c.1402-10348A>C (n.1402-10348A>C) c.2221A>C (p.Asn741His) c.2401A>C (p.Asn801His) c.2068A>C (p.Asn690His) | |
7 | g.117592478A>G | CA368980947 | CFTR | c.2311A>G (p.Asn771Asp) c.*2025A>G (n.*2025A>G) c.2128A>G (p.Asn710Asp) c.*611A>G (n.*611A>G) c.*2135A>G (n.*2135A>G) c.1885A>G (p.Asn629Asp) c.1402-10348A>G (n.1402-10348A>G) c.2221A>G (p.Asn741Asp) c.2401A>G (p.Asn801Asp) c.2068A>G (p.Asn690Asp) | |
7 | g.117592478A>T | CA368980948 | CFTR | c.2311A>T (p.Asn771Tyr) c.*2025A>T (n.*2025A>T) c.2128A>T (p.Asn710Tyr) c.*611A>T (n.*611A>T) c.*2135A>T (n.*2135A>T) c.1885A>T (p.Asn629Tyr) c.1402-10348A>T (n.1402-10348A>T) c.2221A>T (p.Asn741Tyr) c.2401A>T (p.Asn801Tyr) c.2068A>T (p.Asn690Tyr) | |
7 | g.117592479del | CA2695208516 | CFTR | c.2312del (p.Asn771ThrfsTer2) c.*2026del (n.*2026del) c.2129del (p.Asn710ThrfsTer2) c.*612del (n.*612del) c.*2136del (n.*2136del) c.1886del (p.Asn629ThrfsTer2) c.1402-10347del (n.1402-10347del) c.2222del (p.Asn741ThrfsTer2) c.2402del (p.Asn801ThrfsTer2) c.2069del (p.Asn690ThrfsTer2) | |
7 | g.117592479A>C | CA368980950 | CFTR | c.2312A>C (p.Asn771Thr) c.*2026A>C (n.*2026A>C) c.2129A>C (p.Asn710Thr) c.*612A>C (n.*612A>C) c.*2136A>C (n.*2136A>C) c.1886A>C (p.Asn629Thr) c.1402-10347A>C (n.1402-10347A>C) c.2222A>C (p.Asn741Thr) c.2402A>C (p.Asn801Thr) c.2069A>C (p.Asn690Thr) | |
7 | g.117592479A>G | CA368980951 | CFTR | c.2312A>G (p.Asn771Ser) c.*2026A>G (n.*2026A>G) c.2129A>G (p.Asn710Ser) c.*612A>G (n.*612A>G) c.*2136A>G (n.*2136A>G) c.1886A>G (p.Asn629Ser) c.1402-10347A>G (n.1402-10347A>G) c.2222A>G (p.Asn741Ser) c.2402A>G (p.Asn801Ser) c.2069A>G (p.Asn690Ser) | ClinVar gnomAD v4 |
7 | g.117592479A>T | CA368980952 | CFTR | c.2312A>T (p.Asn771Ile) c.*2026A>T (n.*2026A>T) c.2129A>T (p.Asn710Ile) c.*612A>T (n.*612A>T) c.*2136A>T (n.*2136A>T) c.1886A>T (p.Asn629Ile) c.1402-10347A>T (n.1402-10347A>T) c.2222A>T (p.Asn741Ile) c.2402A>T (p.Asn801Ile) c.2069A>T (p.Asn690Ile) | |
7 | g.117592480C>A | CA368980953 | CFTR | c.2313C>A (p.Asn771Lys) c.*2027C>A (n.*2027C>A) c.2130C>A (p.Asn710Lys) c.*613C>A (n.*613C>A) c.*2137C>A (n.*2137C>A) c.1887C>A (p.Asn629Lys) c.1402-10346C>A (n.1402-10346C>A) c.2223C>A (p.Asn741Lys) c.2403C>A (p.Asn801Lys) c.2070C>A (p.Asn690Lys) | |
7 | g.117592480C= | CA1737395254 | CFTR | c.2313C= (p.Asn771=) c.*2027C= (n.*2027C=) c.2130C= (p.Asn710=) c.*613C= (n.*613C=) c.*2137C= (n.*2137C=) c.1887C= (p.Asn629=) c.1402-10346C= (n.1402-10346C=) c.2223C= (p.Asn741=) c.2403C= (p.Asn801=) c.2070C= (p.Asn690=) | |
7 | g.117592480C>G | CA368980954 | CFTR | c.2313C>G (p.Asn771Lys) c.*2027C>G (n.*2027C>G) c.2130C>G (p.Asn710Lys) c.*613C>G (n.*613C>G) c.*2137C>G (n.*2137C>G) c.1887C>G (p.Asn629Lys) c.1402-10346C>G (n.1402-10346C>G) c.2223C>G (p.Asn741Lys) c.2403C>G (p.Asn801Lys) c.2070C>G (p.Asn690Lys) | |
7 | g.117592480C>T | CA4451169 | CFTR | c.2313C>T (p.Asn771=) c.*2027C>T (n.*2027C>T) c.2130C>T (p.Asn710=) c.*613C>T (n.*613C>T) c.*2137C>T (n.*2137C>T) c.1887C>T (p.Asn629=) c.1402-10346C>T (n.1402-10346C>T) c.2223C>T (p.Asn741=) c.2403C>T (p.Asn801=) c.2070C>T (p.Asn690=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |