Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.125317453G>ACA358117071FAT4c.1042G>A (p.Asp348Asn)
c.-55+1476G>A (n.-55+1476G>A)
4g.125317453G>CCA358117072FAT4c.1042G>C (p.Asp348His)
c.-55+1476G>C (n.-55+1476G>C)
4g.125317453G>TCA358117073FAT4c.1042G>T (p.Asp348Tyr)
c.-55+1476G>T (n.-55+1476G>T)
4g.125317454A>CCA358117076FAT4c.1043A>C (p.Asp348Ala)
c.-55+1477A>C (n.-55+1477A>C)
4g.125317454A>GCA358117075FAT4c.1043A>G (p.Asp348Gly)
c.-55+1477A>G (n.-55+1477A>G)
4g.125317454A>TCA358117074FAT4c.1043A>T (p.Asp348Val)
c.-55+1477A>T (n.-55+1477A>T)
gnomAD v4
4g.125317455C>ACA358117078FAT4c.1044C>A (p.Asp348Glu)
c.-55+1478C>A (n.-55+1478C>A)
COSMIC COSMIC
4g.125317455C>GCA358117077FAT4c.1044C>G (p.Asp348Glu)
c.-55+1478C>G (n.-55+1478C>G)
4g.125317455C>TCA441366351FAT4c.1044C>T (p.Asp348=)
c.-55+1478C>T (n.-55+1478C>T)
4g.125317456A>CCA358117079FAT4c.1045A>C (p.Asn349His)
c.-55+1479A>C (n.-55+1479A>C)
4g.125317456A>GCA358117080FAT4c.1045A>G (p.Asn349Asp)
c.-55+1479A>G (n.-55+1479A>G)
4g.125317456A>TCA358117081FAT4c.1045A>T (p.Asn349Tyr)
c.-55+1479A>T (n.-55+1479A>T)
4g.125317457A>CCA358117082FAT4c.1046A>C (p.Asn349Thr)
c.-55+1480A>C (n.-55+1480A>C)
4g.125317457A>GCA358117083FAT4c.1046A>G (p.Asn349Ser)
c.-55+1480A>G (n.-55+1480A>G)
gnomAD v4
4g.125317457A>TCA358117084FAT4c.1046A>T (p.Asn349Ile)
c.-55+1480A>T (n.-55+1480A>T)
4g.125317458T>ACA358117085FAT4c.1047T>A (p.Asn349Lys)
c.-55+1481T>A (n.-55+1481T>A)
4g.125317458T>CCA441366356FAT4c.1047T>C (p.Asn349=)
c.-55+1481T>C (n.-55+1481T>C)
4g.125317458T>GCA358117086FAT4c.1047T>G (p.Asn349Lys)
c.-55+1481T>G (n.-55+1481T>G)
4g.125317459G>ACA358117087FAT4c.1048G>A (p.Asp350Asn)
c.-55+1482G>A (n.-55+1482G>A)
4g.125317459G>CCA358117088FAT4c.1048G>C (p.Asp350His)
c.-55+1482G>C (n.-55+1482G>C)
4g.125317459G>TCA358117089FAT4c.1048G>T (p.Asp350Tyr)
c.-55+1482G>T (n.-55+1482G>T)
4g.125317460A>CCA358117092FAT4c.1049A>C (p.Asp350Ala)
c.-55+1483A>C (n.-55+1483A>C)
4g.125317460A>GCA358117091FAT4c.1049A>G (p.Asp350Gly)
c.-55+1483A>G (n.-55+1483A>G)
4g.125317460A>TCA358117090FAT4c.1049A>T (p.Asp350Val)
c.-55+1483A>T (n.-55+1483A>T)
4g.125317461C>ACA358117093FAT4c.1050C>A (p.Asp350Glu)
c.-55+1484C>A (n.-55+1484C>A)
4g.125317461C=CA1491599892FAT4c.1050C= (p.Asp350=)
c.-55+1484C= (n.-55+1484C=)
4g.125317461C>GCA358117094FAT4c.1050C>G (p.Asp350Glu)
c.-55+1484C>G (n.-55+1484C>G)
4g.125317461C>TCA3071906FAT4c.1050C>T (p.Asp350=)
c.-55+1484C>T (n.-55+1484C>T)
dbSNP ExAC gnomAD v2
4g.125317462C>ACA358117095FAT4c.1051C>A (p.Pro351Thr)
c.-55+1485C>A (n.-55+1485C>A)
4g.125317462C=CA1491599895FAT4c.1051C= (p.Pro351=)
c.-55+1485C= (n.-55+1485C=)
4g.125317462C>GCA3071907FAT4c.1051C>G (p.Pro351Ala)
c.-55+1485C>G (n.-55+1485C>G)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.125317462C>TCA358117096FAT4c.1051C>T (p.Pro351Ser)
c.-55+1485C>T (n.-55+1485C>T)
4g.125317463C>ACA358117097FAT4c.1052C>A (p.Pro351Gln)
c.-55+1486C>A (n.-55+1486C>A)
4g.125317463C=CA1491599901FAT4c.1052C= (p.Pro351=)
c.-55+1486C= (n.-55+1486C=)
4g.125317463C>GCA358117098FAT4c.1052C>G (p.Pro351Arg)
c.-55+1486C>G (n.-55+1486C>G)
dbSNP gnomAD v3 gnomAD v4
4g.125317463C>TCA358117099FAT4c.1052C>T (p.Pro351Leu)
c.-55+1486C>T (n.-55+1486C>T)
gnomAD v4
4g.125317464G>ACA3071908FAT4c.1053G>A (p.Pro351=)
c.-55+1487G>A (n.-55+1487G>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.125317464G>CCA441366362FAT4c.1053G>C (p.Pro351=)
c.-55+1487G>C (n.-55+1487G>C)
dbSNP
4g.125317464G=CA1491599908FAT4c.1053G= (p.Pro351=)
c.-55+1487G= (n.-55+1487G=)
4g.125317464G>TCA441366363FAT4c.1053G>T (p.Pro351=)
c.-55+1487G>T (n.-55+1487G>T)
4g.125317465G>ACA3071909FAT4c.1054G>A (p.Val352Ile)
c.-55+1488G>A (n.-55+1488G>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.125317465G>CCA358117100FAT4c.1054G>C (p.Val352Leu)
c.-55+1488G>C (n.-55+1488G>C)
gnomAD v4
4g.125317465G=CA1491599915FAT4c.1054G= (p.Val352=)
c.-55+1488G= (n.-55+1488G=)
4g.125317465G>TCA358117101FAT4c.1054G>T (p.Val352Leu)
c.-55+1488G>T (n.-55+1488G>T)
4g.125317466T>ACA358117103FAT4c.1055T>A (p.Val352Glu)
c.-55+1489T>A (n.-55+1489T>A)
4g.125317466T>CCA358117104FAT4c.1055T>C (p.Val352Ala)
c.-55+1489T>C (n.-55+1489T>C)
4g.125317466T>GCA358117102FAT4c.1055T>G (p.Val352Gly)
c.-55+1489T>G (n.-55+1489T>G)
4g.125317467A>CCA441366365FAT4c.1056A>C (p.Val352=)
c.-55+1490A>C (n.-55+1490A>C)
4g.125317467A>GCA441366367FAT4c.1056A>G (p.Val352=)
c.-55+1490A>G (n.-55+1490A>G)
gnomAD v4
4g.125317467A>TCA441366366FAT4c.1056A>T (p.Val352=)
c.-55+1490A>T (n.-55+1490A>T)

Number of alleles fetched