| 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.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) |