Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.107689101G>A | CA184789 | SLC26A4 | c.1050G>A (p.Leu350=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.107689101G>C | CA457088419 | SLC26A4 | c.1050G>C (p.Leu350=) | |
7 | g.107689101G= | CA1732747248 | SLC26A4 | c.1050G= (p.Leu350=) | |
7 | g.107689101G>T | CA457088423 | SLC26A4 | c.1050G>T (p.Leu350=) | |
7 | g.107689102G>A | CA368838547 | SLC26A4 | c.1051G>A (p.Ala351Thr) | |
7 | g.107689102G>C | CA368838549 | SLC26A4 | c.1051G>C (p.Ala351Pro) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.107689102G= | CA1732747251 | SLC26A4 | c.1051G= (p.Ala351=) | |
7 | g.107689102G>T | CA368838550 | SLC26A4 | c.1051G>T (p.Ala351Ser) | gnomAD v4 |
7 | g.107689103C>A | CA368838554 | SLC26A4 | c.1052C>A (p.Ala351Asp) | COSMIC |
7 | g.107689103C= | CA1732747255 | SLC26A4 | c.1052C= (p.Ala351=) | |
7 | g.107689103C>G | CA4432668 | SLC26A4 | c.1052C>G (p.Ala351Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.107689103C>T | CA368838555 | SLC26A4 | c.1052C>T (p.Ala351Val) | |
7 | g.107689104T>A | CA457088440 | SLC26A4 | c.1053T>A (p.Ala351=) | |
7 | g.107689104T>C | CA457088441 | SLC26A4 | c.1053T>C (p.Ala351=) | ClinVar |
7 | g.107689104T>G | CA457088445 | SLC26A4 | c.1053T>G (p.Ala351=) | |
7 | g.107689105del | CA2573052787 | SLC26A4 | c.1054del (p.Ala352HisfsTer16) | ClinVar dbSNP |
7 | g.107689105G>A | CA132652 | SLC26A4 | c.1054G>A (p.Ala352Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.107689105G>C | CA368838556 | SLC26A4 | c.1054G>C (p.Ala352Pro) | |
7 | g.107689105G= | CA1732747319 | SLC26A4 | c.1054G= (p.Ala352=) | |
7 | g.107689105G>T | CA368838557 | SLC26A4 | c.1054G>T (p.Ala352Ser) | |
7 | g.107689106C>A | CA368838559 | SLC26A4 | c.1055C>A (p.Ala352Glu) | |
7 | g.107689106C>G | CA368838560 | SLC26A4 | c.1055C>G (p.Ala352Gly) | gnomAD v4 |
7 | g.107689106C>T | CA368838562 | SLC26A4 | c.1055C>T (p.Ala352Val) | |
7 | g.107689107A= | CA1732747322 | SLC26A4 | c.1056A= (p.Ala352=) | |
7 | g.107689107A>C | CA457088462 | SLC26A4 | c.1056A>C (p.Ala352=) | |
7 | g.107689107A>G | CA457088465 | SLC26A4 | c.1056A>G (p.Ala352=) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.107689107A>T | CA457088468 | SLC26A4 | c.1056A>T (p.Ala352=) | |
7 | g.107689108T>A | CA368838564 | SLC26A4 | c.1057T>A (p.Ser353Thr) | |
7 | g.107689108T>C | CA368838565 | SLC26A4 | c.1057T>C (p.Ser353Pro) | |
7 | g.107689108T>G | CA4432669 | SLC26A4 | c.1057T>G (p.Ser353Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.107689108T= | CA1732747327 | SLC26A4 | c.1057T= (p.Ser353=) | |
7 | g.107689109C>A | CA368838568 | SLC26A4 | c.1058C>A (p.Ser353Ter) | |
7 | g.107689109C>G | CA368838569 | SLC26A4 | c.1058C>G (p.Ser353Ter) | ClinVar COSMIC |
7 | g.107689109C>T | CA368838572 | SLC26A4 | c.1058C>T (p.Ser353Leu) | |
7 | g.107689110A= | CA1732747330 | SLC26A4 | c.1059A= (p.Ser353=) | |
7 | g.107689110A>C | CA457088486 | SLC26A4 | c.1059A>C (p.Ser353=) | |
7 | g.107689110A>G | CA457088489 | SLC26A4 | c.1059A>G (p.Ser353=) | |
7 | g.107689110A>T | CA457088492 | SLC26A4 | c.1059A>T (p.Ser353=) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.107689111T>A | CA368838580 | SLC26A4 | c.1060T>A (p.Phe354Ile) | |
7 | g.107689111T>C | CA368838575 | SLC26A4 | c.1060T>C (p.Phe354Leu) | |
7 | g.107689111T>G | CA368838577 | SLC26A4 | c.1060T>G (p.Phe354Val) | |
7 | g.107689112T>A | CA368838582 | SLC26A4 | c.1061T>A (p.Phe354Tyr) | |
7 | g.107689112T>C | CA132656 | SLC26A4 | c.1061T>C (p.Phe354Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.107689112T>G | CA368838583 | SLC26A4 | c.1061T>G (p.Phe354Cys) | |
7 | g.107689112T= | CA1732747337 | SLC26A4 | c.1061T= (p.Phe354=) | |
7 | g.107689113T>A | CA368838585 | SLC26A4 | c.1062T>A (p.Phe354Leu) | |
7 | g.107689113T>C | CA457088514 | SLC26A4 | c.1062T>C (p.Phe354=) | |
7 | g.107689113T>G | CA368838588 | SLC26A4 | c.1062T>G (p.Phe354Leu) | |
7 | g.107689114T>A | CA368838589 | SLC26A4 | c.1063T>A (p.Ser355Thr) | |
7 | g.107689114T>C | CA4432670 | SLC26A4 | c.1063T>C (p.Ser355Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |