| 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.117592362T>A | CA368980346 | CFTR | c.2195T>A (p.Leu732Ter) c.*1909T>A (n.*1909T>A) c.2012T>A (p.Leu671Ter) c.*495T>A (n.*495T>A) c.*2019T>A (n.*2019T>A) c.1769T>A (p.Leu590Ter) c.1402-10464T>A (n.1402-10464T>A) c.2105T>A (p.Leu702Ter) c.2285T>A (p.Leu762Ter) c.1952T>A (p.Leu651Ter) | |
| 7 | g.117592362T>C | CA368980347 | CFTR | c.2195T>C (p.Leu732Ser) c.*1909T>C (n.*1909T>C) c.2012T>C (p.Leu671Ser) c.*495T>C (n.*495T>C) c.*2019T>C (n.*2019T>C) c.1769T>C (p.Leu590Ser) c.1402-10464T>C (n.1402-10464T>C) c.2105T>C (p.Leu702Ser) c.2285T>C (p.Leu762Ser) c.1952T>C (p.Leu651Ser) | |
| 7 | g.117592362T>G | CA328095 | CFTR | c.2195T>G (p.Leu732Ter) c.*1909T>G (n.*1909T>G) c.2012T>G (p.Leu671Ter) c.*495T>G (n.*495T>G) c.*2019T>G (n.*2019T>G) c.1769T>G (p.Leu590Ter) c.1402-10464T>G (n.1402-10464T>G) c.2105T>G (p.Leu702Ter) c.2285T>G (p.Leu762Ter) c.1952T>G (p.Leu651Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.117592362T= | CA1737394995 | CFTR | c.2195T= (p.Leu732=) c.*1909T= (n.*1909T=) c.2012T= (p.Leu671=) c.*495T= (n.*495T=) c.*2019T= (n.*2019T=) c.1769T= (p.Leu590=) c.1402-10464T= (n.1402-10464T=) c.2105T= (p.Leu702=) c.2285T= (p.Leu762=) c.1952T= (p.Leu651=) | |
| 7 | g.117592363A>C | CA368980348 | CFTR | c.2196A>C (p.Leu732Phe) c.*1910A>C (n.*1910A>C) c.2013A>C (p.Leu671Phe) c.*496A>C (n.*496A>C) c.*2020A>C (n.*2020A>C) c.1770A>C (p.Leu590Phe) c.1402-10463A>C (n.1402-10463A>C) c.2106A>C (p.Leu702Phe) c.2286A>C (p.Leu762Phe) c.1953A>C (p.Leu651Phe) | |
| 7 | g.117592363A>G | CA457449416 | CFTR | c.2196A>G (p.Leu732=) c.*1910A>G (n.*1910A>G) c.2013A>G (p.Leu671=) c.*496A>G (n.*496A>G) c.*2020A>G (n.*2020A>G) c.1770A>G (p.Leu590=) c.1402-10463A>G (n.1402-10463A>G) c.2106A>G (p.Leu702=) c.2286A>G (p.Leu762=) c.1953A>G (p.Leu651=) | gnomAD v4 |
| 7 | g.117592363A>T | CA368980349 | CFTR | c.2196A>T (p.Leu732Phe) c.*1910A>T (n.*1910A>T) c.2013A>T (p.Leu671Phe) c.*496A>T (n.*496A>T) c.*2020A>T (n.*2020A>T) c.1770A>T (p.Leu590Phe) c.1402-10463A>T (n.1402-10463A>T) c.2106A>T (p.Leu702Phe) c.2286A>T (p.Leu762Phe) c.1953A>T (p.Leu651Phe) | |
| 7 | g.117592364G>A | CA368980350 | CFTR | c.2197G>A (p.Glu733Lys) c.*1911G>A (n.*1911G>A) c.2014G>A (p.Glu672Lys) c.*497G>A (n.*497G>A) c.*2021G>A (n.*2021G>A) c.1771G>A (p.Glu591Lys) c.1402-10462G>A (n.1402-10462G>A) c.2107G>A (p.Glu703Lys) c.2287G>A (p.Glu763Lys) c.1954G>A (p.Glu652Lys) | |
| 7 | g.117592364G>C | CA368980351 | CFTR | c.2197G>C (p.Glu733Gln) c.*1911G>C (n.*1911G>C) c.2014G>C (p.Glu672Gln) c.*497G>C (n.*497G>C) c.*2021G>C (n.*2021G>C) c.1771G>C (p.Glu591Gln) c.1402-10462G>C (n.1402-10462G>C) c.2107G>C (p.Glu703Gln) c.2287G>C (p.Glu763Gln) c.1954G>C (p.Glu652Gln) | |
| 7 | g.117592364G>T | CA368980352 | CFTR | c.2197G>T (p.Glu733Ter) c.*1911G>T (n.*1911G>T) c.2014G>T (p.Glu672Ter) c.*497G>T (n.*497G>T) c.*2021G>T (n.*2021G>T) c.1771G>T (p.Glu591Ter) c.1402-10462G>T (n.1402-10462G>T) c.2107G>T (p.Glu703Ter) c.2287G>T (p.Glu763Ter) c.1954G>T (p.Glu652Ter) | |
| 7 | g.117592365A>C | CA368980353 | CFTR | c.2198A>C (p.Glu733Ala) c.*1912A>C (n.*1912A>C) c.2015A>C (p.Glu672Ala) c.*498A>C (n.*498A>C) c.*2022A>C (n.*2022A>C) c.1772A>C (p.Glu591Ala) c.1402-10461A>C (n.1402-10461A>C) c.2108A>C (p.Glu703Ala) c.2288A>C (p.Glu763Ala) c.1955A>C (p.Glu652Ala) | |
| 7 | g.117592365A>G | CA368980354 | CFTR | c.2198A>G (p.Glu733Gly) c.*1912A>G (n.*1912A>G) c.2015A>G (p.Glu672Gly) c.*498A>G (n.*498A>G) c.*2022A>G (n.*2022A>G) c.1772A>G (p.Glu591Gly) c.1402-10461A>G (n.1402-10461A>G) c.2108A>G (p.Glu703Gly) c.2288A>G (p.Glu763Gly) c.1955A>G (p.Glu652Gly) | |
| 7 | g.117592365A>T | CA368980358 | CFTR | c.2198A>T (p.Glu733Val) c.*1912A>T (n.*1912A>T) c.2015A>T (p.Glu672Val) c.*498A>T (n.*498A>T) c.*2022A>T (n.*2022A>T) c.1772A>T (p.Glu591Val) c.1402-10461A>T (n.1402-10461A>T) c.2108A>T (p.Glu703Val) c.2288A>T (p.Glu763Val) c.1955A>T (p.Glu652Val) | |
| 7 | g.117592366G>A | CA457449418 | CFTR | c.2199G>A (p.Glu733=) c.*1913G>A (n.*1913G>A) c.2016G>A (p.Glu672=) c.*499G>A (n.*499G>A) c.*2023G>A (n.*2023G>A) c.1773G>A (p.Glu591=) c.1402-10460G>A (n.1402-10460G>A) c.2109G>A (p.Glu703=) c.2289G>A (p.Glu763=) c.1956G>A (p.Glu652=) | |
| 7 | g.117592366G>C | CA368980363 | CFTR | c.2199G>C (p.Glu733Asp) c.*1913G>C (n.*1913G>C) c.2016G>C (p.Glu672Asp) c.*499G>C (n.*499G>C) c.*2023G>C (n.*2023G>C) c.1773G>C (p.Glu591Asp) c.1402-10460G>C (n.1402-10460G>C) c.2109G>C (p.Glu703Asp) c.2289G>C (p.Glu763Asp) c.1956G>C (p.Glu652Asp) | |
| 7 | g.117592366G>T | CA368980360 | CFTR | c.2199G>T (p.Glu733Asp) c.*1913G>T (n.*1913G>T) c.2016G>T (p.Glu672Asp) c.*499G>T (n.*499G>T) c.*2023G>T (n.*2023G>T) c.1773G>T (p.Glu591Asp) c.1402-10460G>T (n.1402-10460G>T) c.2109G>T (p.Glu703Asp) c.2289G>T (p.Glu763Asp) c.1956G>T (p.Glu652Asp) | |
| 7 | g.117592367A>C | CA457449419 | CFTR | c.2200A>C (p.Arg734=) c.*1914A>C (n.*1914A>C) c.2017A>C (p.Arg673=) c.*500A>C (n.*500A>C) c.*2024A>C (n.*2024A>C) c.1774A>C (p.Arg592=) c.1402-10459A>C (n.1402-10459A>C) c.2110A>C (p.Arg704=) c.2290A>C (p.Arg764=) c.1957A>C (p.Arg653=) | |
| 7 | g.117592367A>G | CA368980366 | CFTR | c.2200A>G (p.Arg734Gly) c.*1914A>G (n.*1914A>G) c.2017A>G (p.Arg673Gly) c.*500A>G (n.*500A>G) c.*2024A>G (n.*2024A>G) c.1774A>G (p.Arg592Gly) c.1402-10459A>G (n.1402-10459A>G) c.2110A>G (p.Arg704Gly) c.2290A>G (p.Arg764Gly) c.1957A>G (p.Arg653Gly) | ClinVar gnomAD v4 |
| 7 | g.117592367A>T | CA368980368 | CFTR | c.2200A>T (p.Arg734Ter) c.*1914A>T (n.*1914A>T) c.2017A>T (p.Arg673Ter) c.*500A>T (n.*500A>T) c.*2024A>T (n.*2024A>T) c.1774A>T (p.Arg592Ter) c.1402-10459A>T (n.1402-10459A>T) c.2110A>T (p.Arg704Ter) c.2290A>T (p.Arg764Ter) c.1957A>T (p.Arg653Ter) | |
| 7 | g.117592369_117592371del | CA2684619358 | CFTR | c.2202_2204del (p.Arg735del) c.*1916_*1918del (n.*1916_*1918del) c.2019_2021del (p.Arg674del) c.*502_*504del (n.*502_*504del) c.*2026_*2028del (n.*2026_*2028del) c.1776_1778del (p.Arg593del) c.1402-10457_1402-10455del (n.1402-10457_1402-10455del) c.2112_2114del (p.Arg705del) c.2292_2294del (p.Arg765del) c.1959_1961del (p.Arg654del) | gnomAD v4 |
| 7 | g.117592368G>A | CA368980371 | CFTR | c.2201G>A (p.Arg734Lys) c.*1915G>A (n.*1915G>A) c.2018G>A (p.Arg673Lys) c.*501G>A (n.*501G>A) c.*2025G>A (n.*2025G>A) c.1775G>A (p.Arg592Lys) c.1402-10458G>A (n.1402-10458G>A) c.2111G>A (p.Arg704Lys) c.2291G>A (p.Arg764Lys) c.1958G>A (p.Arg653Lys) | |
| 7 | g.117592368G>C | CA368980373 | CFTR | c.2201G>C (p.Arg734Thr) c.*1915G>C (n.*1915G>C) c.2018G>C (p.Arg673Thr) c.*501G>C (n.*501G>C) c.*2025G>C (n.*2025G>C) c.1775G>C (p.Arg592Thr) c.1402-10458G>C (n.1402-10458G>C) c.2111G>C (p.Arg704Thr) c.2291G>C (p.Arg764Thr) c.1958G>C (p.Arg653Thr) | |
| 7 | g.117592368G>T | CA368980375 | CFTR | c.2201G>T (p.Arg734Ile) c.*1915G>T (n.*1915G>T) c.2018G>T (p.Arg673Ile) c.*501G>T (n.*501G>T) c.*2025G>T (n.*2025G>T) c.1775G>T (p.Arg592Ile) c.1402-10458G>T (n.1402-10458G>T) c.2111G>T (p.Arg704Ile) c.2291G>T (p.Arg764Ile) c.1958G>T (p.Arg653Ile) | |
| 7 | g.117592368_117592369delinsGA | CA1737395000 | CFTR | c.2201_2202delinsGA (p.Arg734=) c.*1915_*1916delinsGA (n.*1915_*1916delinsGA) c.2018_2019delinsGA (p.Arg673=) c.*501_*502delinsGA (n.*501_*502delinsGA) c.*2025_*2026delinsGA (n.*2025_*2026delinsGA) c.1775_1776delinsGA (p.Arg592=) c.1402-10458_1402-10457delinsGA (n.1402-10458_1402-10457delinsGA) c.2111_2112delinsGA (p.Arg704=) c.2291_2292delinsGA (p.Arg764=) c.1958_1959delinsGA (p.Arg653=) | |
| 7 | g.117592369A>C | CA368980378 | CFTR | c.2202A>C (p.Arg734Ser) c.*1916A>C (n.*1916A>C) c.2019A>C (p.Arg673Ser) c.*502A>C (n.*502A>C) c.*2026A>C (n.*2026A>C) c.1776A>C (p.Arg592Ser) c.1402-10457A>C (n.1402-10457A>C) c.2112A>C (p.Arg704Ser) c.2292A>C (p.Arg764Ser) c.1959A>C (p.Arg653Ser) | |
| 7 | g.117592369A>G | CA457449423 | CFTR | c.2202A>G (p.Arg734=) c.*1916A>G (n.*1916A>G) c.2019A>G (p.Arg673=) c.*502A>G (n.*502A>G) c.*2026A>G (n.*2026A>G) c.1776A>G (p.Arg592=) c.1402-10457A>G (n.1402-10457A>G) c.2112A>G (p.Arg704=) c.2292A>G (p.Arg764=) c.1959A>G (p.Arg653=) | ClinVar |
| 7 | g.117592369A>T | CA368980380 | CFTR | c.2202A>T (p.Arg734Ser) c.*1916A>T (n.*1916A>T) c.2019A>T (p.Arg673Ser) c.*502A>T (n.*502A>T) c.*2026A>T (n.*2026A>T) c.1776A>T (p.Arg592Ser) c.1402-10457A>T (n.1402-10457A>T) c.2112A>T (p.Arg704Ser) c.2292A>T (p.Arg764Ser) c.1959A>T (p.Arg653Ser) | |
| 7 | g.117592370del | CA326767 | CFTR | c.2203del (p.Arg735GlyfsTer4) c.*1917del (n.*1917del) c.2020del (p.Arg674GlyfsTer4) c.*503del (n.*503del) c.*2027del (n.*2027del) c.1777del (p.Arg593GlyfsTer4) c.1402-10456del (n.1402-10456del) c.2113del (p.Arg705GlyfsTer4) c.2293del (p.Arg765GlyfsTer4) c.1960del (p.Arg654GlyfsTer4) | ClinVar dbSNP |
| 7 | g.117592370A>C | CA457449427 | CFTR | c.2203A>C (p.Arg735=) c.*1917A>C (n.*1917A>C) c.2020A>C (p.Arg674=) c.*503A>C (n.*503A>C) c.*2027A>C (n.*2027A>C) c.1777A>C (p.Arg593=) c.1402-10456A>C (n.1402-10456A>C) c.2113A>C (p.Arg705=) c.2293A>C (p.Arg765=) c.1960A>C (p.Arg654=) | |
| 7 | g.117592370A>G | CA368980385 | CFTR | c.2203A>G (p.Arg735Gly) c.*1917A>G (n.*1917A>G) c.2020A>G (p.Arg674Gly) c.*503A>G (n.*503A>G) c.*2027A>G (n.*2027A>G) c.1777A>G (p.Arg593Gly) c.1402-10456A>G (n.1402-10456A>G) c.2113A>G (p.Arg705Gly) c.2293A>G (p.Arg765Gly) c.1960A>G (p.Arg654Gly) | |
| 7 | g.117592370A>T | CA368980387 | CFTR | c.2203A>T (p.Arg735Trp) c.*1917A>T (n.*1917A>T) c.2020A>T (p.Arg674Trp) c.*503A>T (n.*503A>T) c.*2027A>T (n.*2027A>T) c.1777A>T (p.Arg593Trp) c.1402-10456A>T (n.1402-10456A>T) c.2113A>T (p.Arg705Trp) c.2293A>T (p.Arg765Trp) c.1960A>T (p.Arg654Trp) | |
| 7 | g.117592370_117592371del | CA2684619359 | CFTR | c.2203_2204del (p.Arg735AlafsTer8) c.*1917_*1918del (n.*1917_*1918del) c.2020_2021del (p.Arg674AlafsTer8) c.*503_*504del (n.*503_*504del) c.*2027_*2028del (n.*2027_*2028del) c.1777_1778del (p.Arg593AlafsTer8) c.1402-10456_1402-10455del (n.1402-10456_1402-10455del) c.2113_2114del (p.Arg705AlafsTer8) c.2293_2294del (p.Arg765AlafsTer8) c.1960_1961del (p.Arg654AlafsTer8) | gnomAD v4 |
| 7 | g.117592371G>A | CA326768 | CFTR | c.2204G>A (p.Arg735Lys) c.*1918G>A (n.*1918G>A) c.2021G>A (p.Arg674Lys) c.*504G>A (n.*504G>A) c.*2028G>A (n.*2028G>A) c.1778G>A (p.Arg593Lys) c.1402-10455G>A (n.1402-10455G>A) c.2114G>A (p.Arg705Lys) c.2294G>A (p.Arg765Lys) c.1961G>A (p.Arg654Lys) | ClinVar dbSNP |
| 7 | g.117592371G>C | CA368980390 | CFTR | c.2204G>C (p.Arg735Thr) c.*1918G>C (n.*1918G>C) c.2021G>C (p.Arg674Thr) c.*504G>C (n.*504G>C) c.*2028G>C (n.*2028G>C) c.1778G>C (p.Arg593Thr) c.1402-10455G>C (n.1402-10455G>C) c.2114G>C (p.Arg705Thr) c.2294G>C (p.Arg765Thr) c.1961G>C (p.Arg654Thr) | |
| 7 | g.117592371G= | CA1737395010 | CFTR | c.2204G= (p.Arg735=) c.*1918G= (n.*1918G=) c.2021G= (p.Arg674=) c.*504G= (n.*504G=) c.*2028G= (n.*2028G=) c.1778G= (p.Arg593=) c.1402-10455G= (n.1402-10455G=) c.2114G= (p.Arg705=) c.2294G= (p.Arg765=) c.1961G= (p.Arg654=) | |
| 7 | g.117592371G>T | CA368980393 | CFTR | c.2204G>T (p.Arg735Met) c.*1918G>T (n.*1918G>T) c.2021G>T (p.Arg674Met) c.*504G>T (n.*504G>T) c.*2028G>T (n.*2028G>T) c.1778G>T (p.Arg593Met) c.1402-10455G>T (n.1402-10455G>T) c.2114G>T (p.Arg705Met) c.2294G>T (p.Arg765Met) c.1961G>T (p.Arg654Met) | gnomAD v4 |
| 7 | g.117592372G>A | CA457449430 | CFTR | c.2205G>A (p.Arg735=) c.*1919G>A (n.*1919G>A) c.2022G>A (p.Arg674=) c.*505G>A (n.*505G>A) c.*2029G>A (n.*2029G>A) c.1779G>A (p.Arg593=) c.1402-10454G>A (n.1402-10454G>A) c.2115G>A (p.Arg705=) c.2295G>A (p.Arg765=) c.1962G>A (p.Arg654=) | |
| 7 | g.117592372G>C | CA368980397 | CFTR | c.2205G>C (p.Arg735Ser) c.*1919G>C (n.*1919G>C) c.2022G>C (p.Arg674Ser) c.*505G>C (n.*505G>C) c.*2029G>C (n.*2029G>C) c.1779G>C (p.Arg593Ser) c.1402-10454G>C (n.1402-10454G>C) c.2115G>C (p.Arg705Ser) c.2295G>C (p.Arg765Ser) c.1962G>C (p.Arg654Ser) | ClinVar dbSNP |
| 7 | g.117592372G>T | CA368980399 | CFTR | c.2205G>T (p.Arg735Ser) c.*1919G>T (n.*1919G>T) c.2022G>T (p.Arg674Ser) c.*505G>T (n.*505G>T) c.*2029G>T (n.*2029G>T) c.1779G>T (p.Arg593Ser) c.1402-10454G>T (n.1402-10454G>T) c.2115G>T (p.Arg705Ser) c.2295G>T (p.Arg765Ser) c.1962G>T (p.Arg654Ser) | |
| 7 | g.117592373C>A | CA368980400 | CFTR | c.2206C>A (p.Leu736Met) c.*1920C>A (n.*1920C>A) c.2023C>A (p.Leu675Met) c.*506C>A (n.*506C>A) c.*2030C>A (n.*2030C>A) c.1780C>A (p.Leu594Met) c.1402-10453C>A (n.1402-10453C>A) c.2116C>A (p.Leu706Met) c.2296C>A (p.Leu766Met) c.1963C>A (p.Leu655Met) | |
| 7 | g.117592373C= | CA1737395012 | CFTR | c.2206C= (p.Leu736=) c.*1920C= (n.*1920C=) c.2023C= (p.Leu675=) c.*506C= (n.*506C=) c.*2030C= (n.*2030C=) c.1780C= (p.Leu594=) c.1402-10453C= (n.1402-10453C=) c.2116C= (p.Leu706=) c.2296C= (p.Leu766=) c.1963C= (p.Leu655=) | |
| 7 | g.117592373C>G | CA368980402 | CFTR | c.2206C>G (p.Leu736Val) c.*1920C>G (n.*1920C>G) c.2023C>G (p.Leu675Val) c.*506C>G (n.*506C>G) c.*2030C>G (n.*2030C>G) c.1780C>G (p.Leu594Val) c.1402-10453C>G (n.1402-10453C>G) c.2116C>G (p.Leu706Val) c.2296C>G (p.Leu766Val) c.1963C>G (p.Leu655Val) | |
| 7 | g.117592373C>T | CA457449433 | CFTR | c.2206C>T (p.Leu736=) c.*1920C>T (n.*1920C>T) c.2023C>T (p.Leu675=) c.*506C>T (n.*506C>T) c.*2030C>T (n.*2030C>T) c.1780C>T (p.Leu594=) c.1402-10453C>T (n.1402-10453C>T) c.2116C>T (p.Leu706=) c.2296C>T (p.Leu766=) c.1963C>T (p.Leu655=) | dbSNP gnomAD v4 |
| 7 | g.117592374T>A | CA368980405 | CFTR | c.2207T>A (p.Leu736Gln) c.*1921T>A (n.*1921T>A) c.2024T>A (p.Leu675Gln) c.*507T>A (n.*507T>A) c.*2031T>A (n.*2031T>A) c.1781T>A (p.Leu594Gln) c.1402-10452T>A (n.1402-10452T>A) c.2117T>A (p.Leu706Gln) c.2297T>A (p.Leu766Gln) c.1964T>A (p.Leu655Gln) | |
| 7 | g.117592374T>C | CA368980407 | CFTR | c.2207T>C (p.Leu736Pro) c.*1921T>C (n.*1921T>C) c.2024T>C (p.Leu675Pro) c.*507T>C (n.*507T>C) c.*2031T>C (n.*2031T>C) c.1781T>C (p.Leu594Pro) c.1402-10452T>C (n.1402-10452T>C) c.2117T>C (p.Leu706Pro) c.2297T>C (p.Leu766Pro) c.1964T>C (p.Leu655Pro) | |
| 7 | g.117592374T>G | CA368980409 | CFTR | c.2207T>G (p.Leu736Arg) c.*1921T>G (n.*1921T>G) c.2024T>G (p.Leu675Arg) c.*507T>G (n.*507T>G) c.*2031T>G (n.*2031T>G) c.1781T>G (p.Leu594Arg) c.1402-10452T>G (n.1402-10452T>G) c.2117T>G (p.Leu706Arg) c.2297T>G (p.Leu766Arg) c.1964T>G (p.Leu655Arg) | |
| 7 | g.117592375G>A | CA457449435 | CFTR | c.2208G>A (p.Leu736=) c.*1922G>A (n.*1922G>A) c.2025G>A (p.Leu675=) c.*508G>A (n.*508G>A) c.*2032G>A (n.*2032G>A) c.1782G>A (p.Leu594=) c.1402-10451G>A (n.1402-10451G>A) c.2118G>A (p.Leu706=) c.2298G>A (p.Leu766=) c.1965G>A (p.Leu655=) | ClinVar |
| 7 | g.117592375G>C | CA457449438 | CFTR | c.2208G>C (p.Leu736=) c.*1922G>C (n.*1922G>C) c.2025G>C (p.Leu675=) c.*508G>C (n.*508G>C) c.*2032G>C (n.*2032G>C) c.1782G>C (p.Leu594=) c.1402-10451G>C (n.1402-10451G>C) c.2118G>C (p.Leu706=) c.2298G>C (p.Leu766=) c.1965G>C (p.Leu655=) | |
| 7 | g.117592375G>T | CA457449441 | CFTR | c.2208G>T (p.Leu736=) c.*1922G>T (n.*1922G>T) c.2025G>T (p.Leu675=) c.*508G>T (n.*508G>T) c.*2032G>T (n.*2032G>T) c.1782G>T (p.Leu594=) c.1402-10451G>T (n.1402-10451G>T) c.2118G>T (p.Leu706=) c.2298G>T (p.Leu766=) c.1965G>T (p.Leu655=) |