Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.67940169T>ACA396375774LCATc.1058A>T (p.His353Leu)
c.156-95A>T
c.796A>T (n.796A>T)
16g.67940169T>CCA283160657LCATc.1058A>G (p.His353Arg)
c.156-95A>G
c.796A>G (n.796A>G)
dbSNP gnomAD v2 gnomAD v4
16g.67940169T>GCA396375775LCATc.1058A>C (p.His353Pro)
c.156-95A>C
c.796A>C (n.796A>C)
16g.67940169T=CA2229563242LCATc.1058A= (p.His353=)
c.156-95A=
c.796A= (n.796A=)
16g.67940170G>ACA396375776LCATc.1057C>T (p.His353Tyr)
c.156-96C>T
c.795C>T (n.795C>T)
16g.67940170G>CCA396375777LCATc.1057C>G (p.His353Asp)
c.156-96C>G
c.795C>G (n.795C>G)
16g.67940170G>TCA396375778LCATc.1057C>A (p.His353Asn)
c.156-96C>A
c.795C>A (n.795C>A)
16g.67940171G>ACA496383947LCATc.1056C>T (p.Asp352=)
c.156-97C>T
c.794C>T (n.794C>T)
16g.67940171G>CCA396375779LCATc.1056C>G (p.Asp352Glu)
c.156-97C>G
c.794C>G (n.794C>G)
16g.67940171G>TCA396375780LCATc.1056C>A (p.Asp352Glu)
c.156-97C>A
c.794C>A (n.794C>A)
16g.67940172T>ACA396375783LCATc.1055A>T (p.Asp352Val)
c.156-98A>T
c.793A>T (n.793A>T)
16g.67940172T>CCA396375782LCATc.1055A>G (p.Asp352Gly)
c.156-98A>G
c.793A>G (n.793A>G)
16g.67940172T>GCA396375781LCATc.1055A>C (p.Asp352Ala)
c.156-98A>C
c.793A>C (n.793A>C)
16g.67940173C>ACA396375784LCATc.1054G>T (p.Asp352Tyr)
c.156-99G>T
c.792G>T (n.792G>T)
gnomAD v4
16g.67940173C=CA2229563243LCATc.1054G= (p.Asp352=)
c.156-99G=
c.792G= (n.792G=)
16g.67940173C>GCA283160668LCATc.1054G>C (p.Asp352His)
c.156-99G>C
c.792G>C (n.792G>C)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.67940173C>TCA8120903LCATc.1054G>A (p.Asp352Asn)
c.156-99G>A
c.792G>A (n.792G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.67940174G>ACA8120904LCATc.1053C>T (p.Tyr351=)
c.156-100C>T
c.791C>T (n.791C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.67940174G>CCA396375785LCATc.1053C>G (p.Tyr351Ter)
c.156-100C>G
c.791C>G (n.791C>G)
16g.67940174G=CA2229563244LCATc.1053C= (p.Tyr351=)
c.156-100C=
c.791C= (n.791C=)
16g.67940174G>TCA396375786LCATc.1053C>A (p.Tyr351Ter)
c.156-100C>A
c.791C>A (n.791C>A)
16g.67940175T>ACA396375787LCATc.1052A>T (p.Tyr351Phe)
c.156-101A>T
c.790A>T (n.790A>T)
16g.67940175T>CCA396375788LCATc.1052A>G (p.Tyr351Cys)
c.156-101A>G
c.790A>G (n.790A>G)
gnomAD v4
16g.67940175T>GCA396375789LCATc.1052A>C (p.Tyr351Ser)
c.156-101A>C
c.790A>C (n.790A>C)
16g.67940176A>CCA396375790LCATc.1051T>G (p.Tyr351Asp)
c.156-102T>G
c.789T>G (n.789T>G)
16g.67940176A>GCA396375791LCATc.1051T>C (p.Tyr351His)
c.156-102T>C
c.789T>C (n.789T>C)
16g.67940176A>TCA396375792LCATc.1051T>A (p.Tyr351Asn)
c.156-102T>A
c.789T>A (n.789T>A)
16g.67940177G>ACA496383953LCATc.1050C>T (p.Ile350=)
c.156-103C>T
c.788C>T (n.788C>T)
16g.67940177G>CCA396375793LCATc.1050C>G (p.Ile350Met)
c.156-103C>G
c.788C>G (n.788C>G)
16g.67940177G>TCA496383954LCATc.1050C>A (p.Ile350=)
c.156-103C>A
c.788C>A (n.788C>A)
16g.67940178A>CCA396375796LCATc.1049T>G (p.Ile350Ser)
c.156-104T>G
c.787T>G (n.787T>G)
16g.67940178A>GCA396375795LCATc.1049T>C (p.Ile350Thr)
c.156-104T>C
c.787T>C (n.787T>C)
16g.67940178A>TCA396375794LCATc.1049T>A (p.Ile350Asn)
c.156-104T>A
c.787T>A (n.787T>A)
16g.67940179T>ACA396375797LCATc.1048A>T (p.Ile350Phe)
c.156-105A>T
c.786A>T (n.786A>T)
16g.67940179T>CCA396375799LCATc.1048A>G (p.Ile350Val)
c.156-105A>G
c.786A>G (n.786A>G)
16g.67940179T>GCA396375798LCATc.1048A>C (p.Ile350Leu)
c.156-105A>C
c.786A>C (n.786A>C)
16g.67940180G>ACA496383955LCATc.1047C>T (p.Tyr349=)
c.156-106C>T
c.785C>T (n.785C>T)
gnomAD v4
16g.67940180G>CCA396375800LCATc.1047C>G (p.Tyr349Ter)
c.156-106C>G
c.785C>G (n.785C>G)
16g.67940180G>TCA396375801LCATc.1047C>A (p.Tyr349Ter)
c.156-106C>A
c.785C>A (n.785C>A)
16g.67940181T>ACA396375802LCATc.1046A>T (p.Tyr349Phe)
c.156-107A>T
c.784A>T (n.784A>T)
16g.67940181T>CCA396375803LCATc.1046A>G (p.Tyr349Cys)
c.156-107A>G
c.784A>G (n.784A>G)
16g.67940181T>GCA396375804LCATc.1046A>C (p.Tyr349Ser)
c.156-107A>C
c.784A>C (n.784A>C)
16g.67940182A>CCA396375805LCATc.1045T>G (p.Tyr349Asp)
c.156-108T>G
c.783T>G (n.783T>G)
16g.67940182A>GCA396375806LCATc.1045T>C (p.Tyr349His)
c.156-108T>C
c.783T>C (n.783T>C)
16g.67940182A>TCA396375807LCATc.1045T>A (p.Tyr349Asn)
c.156-108T>A
c.783T>A (n.783T>A)
16g.67940183G>ACA496383959LCATc.1044C>T (p.Thr348=)
c.156-109C>T
c.782C>T (n.782C>T)
16g.67940183G>CCA496383960LCATc.1044C>G (p.Thr348=)
c.156-109C>G
c.782C>G (n.782C>G)
gnomAD v4
16g.67940183G=CA2229563245LCATc.1044C= (p.Thr348=)
c.156-109C=
c.782C= (n.782C=)
16g.67940183G>TCA8120905LCATc.1044C>A (p.Thr348=)
c.156-109C>A
c.782C>A (n.782C>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.67940184G>ACA396375808LCATc.1043C>T (p.Thr348Ile)
c.156-110C>T
c.781C>T (n.781C>T)
gnomAD v4
16g.67940184G>CCA396375809LCATc.1043C>G (p.Thr348Ser)
c.156-110C>G
c.781C>G (n.781C>G)
16g.67940184G>TCA396375810LCATc.1043C>A (p.Thr348Asn)
c.156-110C>A
c.781C>A (n.781C>A)
16g.67940185T>ACA396375813LCATc.1042A>T (p.Thr348Ser)
c.156-111A>T
c.780A>T (n.780A>T)
16g.67940185T>CCA396375812LCATc.1042A>G (p.Thr348Ala)
c.156-111A>G
c.780A>G (n.780A>G)
gnomAD v4
16g.67940185T>GCA396375811LCATc.1042A>C (p.Thr348Pro)
c.156-111A>C
c.780A>C (n.780A>C)
16g.67940186G>ACA496383963LCATc.1041C>T (p.Arg347=)
c.156-112C>T
c.779C>T (n.779C>T)
dbSNP gnomAD v2 gnomAD v4
16g.67940186G>CCA496383966LCATc.1041C>G (p.Arg347=)
c.156-112C>G
c.779C>G (n.779C>G)
16g.67940186G=CA2229563246LCATc.1041C= (p.Arg347=)
c.156-112C=
c.779C= (n.779C=)
16g.67940186G>TCA496383968LCATc.1041C>A (p.Arg347=)
c.156-112C>A
c.779C>A (n.779C>A)
16g.67940187C>ACA396375814LCATc.1040G>T (p.Arg347Leu)
c.156-113G>T
c.778G>T (n.778G>T)
16g.67940187C=CA2229563247LCATc.1040G= (p.Arg347=)
c.156-113G=
c.778G= (n.778G=)
16g.67940187C>GCA396375815LCATc.1040G>C (p.Arg347Pro)
c.156-113G>C
c.778G>C (n.778G>C)
16g.67940187C>TCA8120907LCATc.1040G>A (p.Arg347His)
c.156-113G>A
c.778G>A (n.778G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.67940188G>ACA8120908LCATc.1039C>T (p.Arg347Cys)
c.156-114C>T
c.777C>T (n.777C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.67940188G>CCA396375816LCATc.1039C>G (p.Arg347Gly)
c.156-114C>G
c.777C>G (n.777C>G)
dbSNP gnomAD v3 gnomAD v4
16g.67940188G=CA2229563248LCATc.1039C= (p.Arg347=)
c.156-114C=
c.777C= (n.777C=)
16g.67940188G>TCA396375817LCATc.1039C>A (p.Arg347Ser)
c.156-114C>A
c.777C>A (n.777C>A)
16g.67940191_67940192insGGGGGGCA8120906LCATc.1039_1040insCCCCCC (p.Pro346_Arg347insProPro)
c.156-114_156-113insCCCCCC
c.777_778insCCCCCC (n.777_778insCCCCCC)
dbSNP ExAC gnomAD v2 gnomAD v4
16g.67940191_67940192insGGGGGGGCA623122338LCATc.1039_1040insCCCCCCC (p.Arg347ProfsTer22)
c.156-114_156-113insCCCCCCC
c.777_778insCCCCCCC (n.777_778insCCCCCCC)
gnomAD v2
16g.67940191_67940192insGGGGGGGGCA919730845LCATc.1039_1040insCCCCCCCC (p.Arg347ProfsTer?)
c.156-114_156-113insCCCCCCCC
c.777_778insCCCCCCCC (n.777_778insCCCCCCCC)
dbSNP
16g.67940191delCA645584338LCATc.1039del (p.Arg347AlafsTer?)
c.156-114del
c.777del (n.777del)
COSMIC
16g.67940189G>ACA496383972LCATc.1038C>T (p.Pro346=)
c.156-115C>T
c.776C>T (n.776C>T)
16g.67940189G>CCA496383974LCATc.1038C>G (p.Pro346=)
c.156-115C>G
c.776C>G (n.776C>G)
16g.67940189G>TCA496383975LCATc.1038C>A (p.Pro346=)
c.156-115C>A
c.776C>A (n.776C>A)
16g.67940191_67940201delCA623122339LCATc.1028_1038del (p.Leu343ProfsTer20)
c.156-125_156-115del
c.766_776del (n.766_776del)
gnomAD v2 gnomAD v4
16g.67940190G>ACA396375818LCATc.1037C>T (p.Pro346Leu)
c.156-116C>T
c.775C>T (n.775C>T)
16g.67940190G>CCA396375819LCATc.1037C>G (p.Pro346Arg)
c.156-116C>G
c.775C>G (n.775C>G)
16g.67940190G>TCA396375820LCATc.1037C>A (p.Pro346His)
c.156-116C>A
c.775C>A (n.775C>A)
16g.67940190_67940211delCA2633850829LCATc.1016_1037del (p.Tyr339SerfsTer?)
c.156-137_156-116del
c.754_775del (n.754_775del)
gnomAD v4
16g.67940191_67940219delCA2633850830LCATc.1009_1037del (p.Cys337ProfsTer20)
c.156-144_156-116del
c.747_775del (n.747_775del)
gnomAD v4
16g.67940191G>ACA396375821LCATc.1036C>T (p.Pro346Ser)
c.156-117C>T
c.774C>T (n.774C>T)
16g.67940191G>CCA396375822LCATc.1036C>G (p.Pro346Ala)
c.156-117C>G
c.774C>G (n.774C>G)
16g.67940191G>TCA396375823LCATc.1036C>A (p.Pro346Thr)
c.156-117C>A
c.774C>A (n.774C>A)
16g.67940192_67940215delCA2633850835LCATc.1013_1036del (p.Leu338_Thr345del)
c.156-140_156-117del
c.751_774del (n.751_774del)
gnomAD v4
16g.67940192C>ACA496383978LCATc.1035G>T (p.Thr345=)
c.156-118G>T
c.773G>T (n.773G>T)
16g.67940192C=CA2229563249LCATc.1035G= (p.Thr345=)
c.156-118G=
c.773G= (n.773G=)
16g.67940192C>GCA8120910LCATc.1035G>C (p.Thr345=)
c.156-118G>C
c.773G>C (n.773G>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
16g.67940192C>TCA8120909LCATc.1035G>A (p.Thr345=)
c.156-118G>A
c.773G>A (n.773G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.67940194_67940207delCA2633850841LCATc.1022_1035del (p.Val341AlafsTer21)
c.156-131_156-118del
c.760_773del (n.760_773del)
gnomAD v4
16g.67940193G>ACA116425LCATc.1034C>T (p.Thr345Met)
c.156-119C>T
c.772C>T (n.772C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.67940193G>CCA396375824LCATc.1034C>G (p.Thr345Arg)
c.156-119C>G
c.772C>G (n.772C>G)
16g.67940193G=CA2229563250LCATc.1034C= (p.Thr345=)
c.156-119C=
c.772C= (n.772C=)
16g.67940193G>TCA283160725LCATc.1034C>A (p.Thr345Lys)
c.156-119C>A
c.772C>A (n.772C>A)
dbSNP gnomAD v2 gnomAD v4
16g.67940194_67940201delCA2633850850LCATc.1027_1034del (p.Leu343AlafsTer21)
c.156-126_156-119del
c.765_772del (n.765_772del)
gnomAD v4
16g.67940194T>ACA396375825LCATc.1033A>T (p.Thr345Ser)
c.156-120A>T
c.771A>T (n.771A>T)
16g.67940194T>CCA396375826LCATc.1033A>G (p.Thr345Ala)
c.156-120A>G
c.771A>G (n.771A>G)
gnomAD v4
16g.67940194T>GCA8120911LCATc.1033A>C (p.Thr345Pro)
c.156-120A>C
c.771A>C (n.771A>C)
dbSNP ExAC gnomAD v2 gnomAD v4
16g.67940194T=CA2229563251LCATc.1033A= (p.Thr345=)
c.156-120A=
c.771A= (n.771A=)
16g.67940195G>ACA496383981LCATc.1032C>T (p.Pro344=)
c.156-121C>T
c.770C>T (n.770C>T)
dbSNP gnomAD v4
16g.67940195G>CCA496383982LCATc.1032C>G (p.Pro344=)
c.156-121C>G
c.770C>G (n.770C>G)
16g.67940195G=CA2229563252LCATc.1032C= (p.Pro344=)
c.156-121C=
c.770C= (n.770C=)
16g.67940195G>TCA496383983LCATc.1032C>A (p.Pro344=)
c.156-121C>A
c.770C>A (n.770C>A)
16g.67940196_67940210delCA2633850859LCATc.1018_1032del (p.Gly340_Pro344del)
c.156-135_156-121del
c.756_770del (n.756_770del)
gnomAD v4
16g.67940196G>ACA396375827LCATc.1031C>T (p.Pro344Leu)
c.156-122C>T
c.769C>T (n.769C>T)
gnomAD v4
16g.67940196G>CCA396375828LCATc.1031C>G (p.Pro344Arg)
c.156-122C>G
c.769C>G (n.769C>G)
gnomAD v4
16g.67940196G=CA2229563253LCATc.1031C= (p.Pro344=)
c.156-122C=
c.769C= (n.769C=)
16g.67940196G>TCA8120912LCATc.1031C>A (p.Pro344His)
c.156-122C>A
c.769C>A (n.769C>A)
dbSNP ExAC gnomAD v2 gnomAD v4
16g.67940197_67940207delCA2633850861LCATc.1021_1031del (p.Val341HisfsTer22)
c.156-132_156-122del
c.759_769del (n.759_769del)
gnomAD v4
16g.67940197_67940210delCA2576033442LCATc.1018_1031del (p.Gly340HisfsTer22)
c.156-135_156-122del
c.756_769del (n.756_769del)
16g.67940197G>ACA396375829LCATc.1030C>T (p.Pro344Ser)
c.156-123C>T
c.768C>T (n.768C>T)
dbSNP gnomAD v4
16g.67940197G>CCA396375830LCATc.1030C>G (p.Pro344Ala)
c.156-123C>G
c.768C>G (n.768C>G)
16g.67940197G=CA2229563256LCATc.1030C= (p.Pro344=)
c.156-123C=
c.768C= (n.768C=)
16g.67940197G>TCA396375831LCATc.1030C>A (p.Pro344Thr)
c.156-123C>A
c.768C>A (n.768C>A)
16g.67940197_67940199delinsGCACA2229563254LCATc.1028_1030delinsTGC (p.Leu343=)
c.156-125_156-123delinsTGC
c.766_768delinsTGC (n.766_768delinsTGC)
16g.67940197_67940204delCA2633850865LCATc.1023_1030del (p.Gly342HisfsTer22)
c.156-130_156-123del
c.761_768del (n.761_768del)
gnomAD v4
16g.67940197_67940211delCA2580091816LCATc.1016_1030del (p.Tyr339_Pro344delinsSer)
c.156-137_156-123del
c.754_768del (n.754_768del)
ClinVar
16g.67940197_67940246delinsGCAGGCCCACGCCGTAAAGACAGTATACTTCCACACCAGGTGCTGGGAGTCA2229563255LCATc.981_1030delinsACTCCCAGCACCTGGTGTGGAAGTATACTGTCTTTACGGCGTGGGCCTGC (p.Gly327=)
c.156-172_156-123delinsACTCCCAGCACCTGGTGTGGAAGTATACTGTCTTTACGGCGTGGGCCTGC
c.719_768delinsACTCCCAGCACCTGGTGTGGAAGTATACTGTCTTTACGGCGTGGGCCTGC (n.719_768delinsACTCCCAGCACCTGGTGTGGAAGTATACTGTCTTTACGGCGTGGGCCTGC)
16g.67940198delCA2695223581LCATc.1029del (p.Thr345ArgfsTer?)
c.156-124del
c.767del (n.767del)
16g.67940198C>ACA496383989LCATc.1029G>T (p.Leu343=)
c.156-124G>T
c.767G>T (n.767G>T)
16g.67940198C=CA2229563257LCATc.1029G= (p.Leu343=)
c.156-124G=
c.767G= (n.767G=)
16g.67940198C>GCA496383990LCATc.1029G>C (p.Leu343=)
c.156-124G>C
c.767G>C (n.767G>C)
dbSNP gnomAD v2 gnomAD v4
16g.67940198C>TCA496383991LCATc.1029G>A (p.Leu343=)
c.156-124G>A
c.767G>A (n.767G>A)
16g.67940198_67940199delCA8120913LCATc.1028_1029del (p.Leu343ProfsTer23)
c.156-125_156-124del
c.766_767del (n.766_767del)
dbSNP ExAC gnomAD v4
16g.67940200_67940205delCA496383988LCATc.1024_1029del (p.Gly342_Leu343del)
c.156-129_156-124del
c.762_767del (n.762_767del)
16g.67940199_67940247delCA723097333LCATc.981_1029del (p.Leu328ProfsTer?)
c.156-172_156-124del
c.719_767del (n.719_767del)
dbSNP gnomAD v3 gnomAD v4
16g.67940199A=CA2229563258LCATc.1028T= (p.Leu343=)
c.156-125T=
c.766T= (n.766T=)
16g.67940199A>CCA396375834LCATc.1028T>G (p.Leu343Arg)
c.156-125T>G
c.766T>G (n.766T>G)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.67940199A>GCA396375832LCATc.1028T>C (p.Leu343Pro)
c.156-125T>C
c.766T>C (n.766T>C)
dbSNP gnomAD v4
16g.67940199A>TCA396375833LCATc.1028T>A (p.Leu343Gln)
c.156-125T>A
c.766T>A (n.766T>A)
16g.67940199_67940200delinsCTCA2573054257LCATc.1027_1028delinsAG (p.Leu343Arg)
c.156-126_156-125delinsAG
c.765_766delinsAG (n.765_766delinsAG)
ClinVar
16g.67940200G>ACA8120914LCATc.1027C>T (p.Leu343=)
c.156-126C>T
c.765C>T (n.765C>T)
dbSNP ExAC gnomAD v2 gnomAD v4
16g.67940200G>CCA396375835LCATc.1027C>G (p.Leu343Val)
c.156-126C>G
c.765C>G (n.765C>G)
16g.67940200G=CA2229563259LCATc.1027C= (p.Leu343=)
c.156-126C=
c.765C= (n.765C=)
16g.67940200G>TCA396375836LCATc.1027C>A (p.Leu343Met)
c.156-126C>A
c.765C>A (n.765C>A)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.67940200_67940202delCA623122340LCATc.1025_1027del (p.Gly342_Leu343delinsVal)
c.156-128_156-126del
c.763_765del (n.763_765del)
gnomAD v2 gnomAD v4
16g.67940201G>ACA496383997LCATc.1026C>T (p.Gly342=)
c.156-127C>T
c.764C>T (n.764C>T)
16g.67940201G>CCA496383998LCATc.1026C>G (p.Gly342=)
c.156-127C>G
c.764C>G (n.764C>G)
gnomAD v4
16g.67940201G>TCA496383999LCATc.1026C>A (p.Gly342=)
c.156-127C>A
c.764C>A (n.764C>A)
16g.67940202C>ACA396375837LCATc.1025G>T (p.Gly342Val)
c.156-128G>T
c.763G>T (n.763G>T)
gnomAD v4
16g.67940202C>GCA396375838LCATc.1025G>C (p.Gly342Ala)
c.156-128G>C
c.763G>C (n.763G>C)
16g.67940202C>TCA396375839LCATc.1025G>A (p.Gly342Asp)
c.156-128G>A
c.763G>A (n.763G>A)
16g.67940203C>ACA396375840LCATc.1024G>T (p.Gly342Cys)
c.156-129G>T
c.762G>T (n.762G>T)
16g.67940203C>GCA396375841LCATc.1024G>C (p.Gly342Arg)
c.156-129G>C
c.762G>C (n.762G>C)
COSMIC
16g.67940203C>TCA396375842LCATc.1024G>A (p.Gly342Ser)
c.156-129G>A
c.762G>A (n.762G>A)
16g.67940204C>ACA496384002LCATc.1023G>T (p.Val341=)
c.156-130G>T
c.761G>T (n.761G>T)
16g.67940204C>GCA496384003LCATc.1023G>C (p.Val341=)
c.156-130G>C
c.761G>C (n.761G>C)
16g.67940204C>TCA496384004LCATc.1023G>A (p.Val341=)
c.156-130G>A
c.761G>A (n.761G>A)
COSMIC
16g.67940205A>CCA396375843LCATc.1022T>G (p.Val341Gly)
c.156-131T>G
c.760T>G (n.760T>G)
dbSNP
16g.67940205A>GCA396375844LCATc.1022T>C (p.Val341Ala)
c.156-131T>C
c.760T>C (n.760T>C)
COSMIC
16g.67940205A>TCA396375845LCATc.1022T>A (p.Val341Glu)
c.156-131T>A
c.760T>A (n.760T>A)
16g.67940206C>ACA396375847LCATc.1021G>T (p.Val341Leu)
c.156-132G>T
c.759G>T (n.759G>T)
16g.67940206C=CA2229563260LCATc.1021G= (p.Val341=)
c.156-132G=
c.759G= (n.759G=)
16g.67940206C>GCA396375846LCATc.1021G>C (p.Val341Leu)
c.156-132G>C
c.759G>C (n.759G>C)
COSMIC
16g.67940206C>TCA8120915LCATc.1021G>A (p.Val341Met)
c.156-132G>A
c.759G>A (n.759G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.67940207G>ACA8120916LCATc.1020C>T (p.Gly340=)
c.156-133C>T
c.758C>T (n.758C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.67940207G>CCA496384010LCATc.1020C>G (p.Gly340=)
c.156-133C>G
c.758C>G (n.758C>G)
16g.67940207G=CA2229563261LCATc.1020C= (p.Gly340=)
c.156-133C=
c.758C= (n.758C=)
16g.67940207G>TCA496384007LCATc.1020C>A (p.Gly340=)
c.156-133C>A
c.758C>A (n.758C>A)
gnomAD v4
16g.67940208C>ACA396375850LCATc.1019G>T (p.Gly340Val)
c.156-134G>T
c.757G>T (n.757G>T)
16g.67940208C>GCA396375848LCATc.1019G>C (p.Gly340Ala)
c.156-134G>C
c.757G>C (n.757G>C)
16g.67940208C>TCA396375849LCATc.1019G>A (p.Gly340Asp)
c.156-134G>A
c.757G>A (n.757G>A)
16g.67940210_67940233delCA2633850898LCATc.996_1019del (p.Val333_Gly340del)
c.156-157_156-134del
c.734_757del (n.734_757del)
gnomAD v4
16g.67940209C>ACA283160762LCATc.1018G>T (p.Gly340Cys)
c.156-135G>T
c.756G>T (n.756G>T)
dbSNP
16g.67940209C=CA2229563262LCATc.1018G= (p.Gly340=)
c.156-135G=
c.756G= (n.756G=)
16g.67940209C>GCA396375851LCATc.1018G>C (p.Gly340Arg)
c.156-135G>C
c.756G>C (n.756G>C)
16g.67940209C>TCA396375852LCATc.1018G>A (p.Gly340Ser)
c.156-135G>A
c.756G>A (n.756G>A)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.67940210G>ACA8120917LCATc.1017C>T (p.Tyr339=)
c.156-136C>T
c.755C>T (n.755C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.67940210G>CCA396375854LCATc.1017C>G (p.Tyr339Ter)
c.156-136C>G
c.755C>G (n.755C>G)
16g.67940210G=CA2229563263LCATc.1017C= (p.Tyr339=)
c.156-136C=
c.755C= (n.755C=)
16g.67940210G>TCA396375853LCATc.1017C>A (p.Tyr339Ter)
c.156-136C>A
c.755C>A (n.755C>A)
dbSNP gnomAD v2
16g.67940211T>ACA396375855LCATc.1016A>T (p.Tyr339Phe)
c.156-137A>T
c.754A>T (n.754A>T)
16g.67940211T>CCA396375856LCATc.1016A>G (p.Tyr339Cys)
c.156-137A>G
c.754A>G (n.754A>G)
16g.67940211T>GCA396375857LCATc.1016A>C (p.Tyr339Ser)
c.156-137A>C
c.754A>C (n.754A>C)
16g.67940212A=CA2229563264LCATc.1015T= (p.Tyr339=)
c.156-138T=
c.753T= (n.753T=)
16g.67940212A>CCA396375858LCATc.1015T>G (p.Tyr339Asp)
c.156-138T>G
c.753T>G (n.753T>G)
16g.67940212A>GCA8120918LCATc.1015T>C (p.Tyr339His)
c.156-138T>C
c.753T>C (n.753T>C)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.67940212A>TCA396375859LCATc.1015T>A (p.Tyr339Asn)
c.156-138T>A
c.753T>A (n.753T>A)
16g.67940213A>CCA496384014LCATc.1014T>G (p.Leu338=)
c.156-139T>G
c.752T>G (n.752T>G)
16g.67940213A>GCA496384016LCATc.1014T>C (p.Leu338=)
c.156-139T>C
c.752T>C (n.752T>C)
16g.67940213A>TCA496384015LCATc.1014T>A (p.Leu338=)
c.156-139T>A
c.752T>A (n.752T>A)
16g.67940214A=CA2229563265LCATc.1013T= (p.Leu338=)
c.156-140T=
c.751T= (n.751T=)
16g.67940214A>CCA396375860LCATc.1013T>G (p.Leu338Arg)
c.156-140T>G
c.751T>G (n.751T>G)
16g.67940214A>GCA396375862LCATc.1013T>C (p.Leu338Pro)
c.156-140T>C
c.751T>C (n.751T>C)
gnomAD v4
16g.67940214A>TCA396375861LCATc.1013T>A (p.Leu338His)
c.156-140T>A
c.751T>A (n.751T>A)
dbSNP gnomAD v3 gnomAD v4
16g.67940215G>ACA396375863LCATc.1012C>T (p.Leu338Phe)
c.156-141C>T
c.750C>T (n.750C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.67940215G>CCA396375864LCATc.1012C>G (p.Leu338Val)
c.156-141C>G
c.750C>G (n.750C>G)
16g.67940215G=CA2229563266LCATc.1012C= (p.Leu338=)
c.156-141C=
c.750C= (n.750C=)
16g.67940215G>TCA396375865LCATc.1012C>A (p.Leu338Ile)
c.156-141C>A
c.750C>A (n.750C>A)
16g.67940216A=CA2229563267LCATc.1011T= (p.Cys337=)
c.156-142T=
c.749T= (n.749T=)
16g.67940216A>CCA396375866LCATc.1011T>G (p.Cys337Trp)
c.156-142T>G
c.749T>G (n.749T>G)
16g.67940216A>GCA496384021LCATc.1011T>C (p.Cys337=)
c.156-142T>C
c.749T>C (n.749T>C)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.67940216A>TCA396375867LCATc.1011T>A (p.Cys337Ter)
c.156-142T>A
c.749T>A (n.749T>A)
dbSNP
16g.67940217C>ACA396375868LCATc.1010G>T (p.Cys337Phe)
c.156-143G>T
c.748G>T (n.748G>T)
16g.67940217C>GCA396375869LCATc.1010G>C (p.Cys337Ser)
c.156-143G>C
c.748G>C (n.748G>C)
16g.67940217C>TCA396375870LCATc.1010G>A (p.Cys337Tyr)
c.156-143G>A
c.748G>A (n.748G>A)
16g.67940218A=CA2229563268LCATc.1009T= (p.Cys337=)
c.156-144T=
c.747T= (n.747T=)
16g.67940218A>CCA396375871LCATc.1009T>G (p.Cys337Gly)
c.156-144T>G
c.747T>G (n.747T>G)
16g.67940218A>GCA396375872LCATc.1009T>C (p.Cys337Arg)
c.156-144T>C
c.747T>C (n.747T>C)
dbSNP gnomAD v2 gnomAD v4
16g.67940218A>TCA396375873LCATc.1009T>A (p.Cys337Ser)
c.156-144T>A
c.747T>A (n.747T>A)
16g.67940218_67940219delCA2576033447LCATc.1008_1009del (p.Tyr336Ter)
c.156-145_156-144del
c.746_747del (n.746_747del)
16g.67940219G>ACA496384026LCATc.1008C>T (p.Tyr336=)
c.156-145C>T
c.746C>T (n.746C>T)
16g.67940219G>CCA396375875LCATc.1008C>G (p.Tyr336Ter)
c.156-145C>G
c.746C>G (n.746C>G)
16g.67940219G>TCA396375874LCATc.1008C>A (p.Tyr336Ter)
c.156-145C>A
c.746C>A (n.746C>A)
16g.67940220T>ACA396375876LCATc.1007A>T (p.Tyr336Phe)
c.156-146A>T
c.745A>T (n.745A>T)
16g.67940220T>CCA396375877LCATc.1007A>G (p.Tyr336Cys)
c.156-146A>G
c.745A>G (n.745A>G)
COSMIC
16g.67940220T>GCA396375878LCATc.1007A>C (p.Tyr336Ser)
c.156-146A>C
c.745A>C (n.745A>C)
16g.67940222_67940223delCA2633850912LCATc.1006_1007del (p.Tyr336LeufsTer30)
c.156-147_156-146del
c.744_745del (n.744_745del)
gnomAD v4
16g.67940221A>CCA396375879LCATc.1006T>G (p.Tyr336Asp)
c.156-147T>G
c.744T>G (n.744T>G)
16g.67940221A>GCA396375880LCATc.1006T>C (p.Tyr336His)
c.156-147T>C
c.744T>C (n.744T>C)
16g.67940221A>TCA396375881LCATc.1006T>A (p.Tyr336Asn)
c.156-147T>A
c.744T>A (n.744T>A)
16g.67940222T>ACA496384074LCATc.1005A>T (p.Val335=)
c.156-148A>T
c.743A>T (n.743A>T)
16g.67940222T>CCA496384075LCATc.1005A>G (p.Val335=)
c.156-148A>G
c.743A>G (n.743A>G)
16g.67940222T>GCA8120919LCATc.1005A>C (p.Val335=)
c.156-148A>C
c.743A>C (n.743A>C)
dbSNP ExAC gnomAD v2 gnomAD v4
16g.67940222T=CA2229563269LCATc.1005A= (p.Val335=)
c.156-148A=
c.743A= (n.743A=)
16g.67940223A>CCA396375884LCATc.1004T>G (p.Val335Gly)
c.156-149T>G
c.742T>G (n.742T>G)
16g.67940223A>GCA396375882LCATc.1004T>C (p.Val335Ala)
c.156-149T>C
c.742T>C (n.742T>C)
16g.67940223A>TCA396375883LCATc.1004T>A (p.Val335Glu)
c.156-149T>A
c.742T>A (n.742T>A)
16g.67940224C>ACA396375885LCATc.1003G>T (p.Val335Leu)
c.156-150G>T
c.741G>T (n.741G>T)
16g.67940224C>GCA396375886LCATc.1003G>C (p.Val335Leu)
c.156-150G>C
c.741G>C (n.741G>C)
16g.67940224C>TCA396375887LCATc.1003G>A (p.Val335Ile)
c.156-150G>A
c.741G>A (n.741G>A)
gnomAD v4
16g.67940225T>ACA396375888LCATc.1002A>T (p.Glu334Asp)
c.156-151A>T
c.740A>T (n.740A>T)
16g.67940225T>CCA496384076LCATc.1002A>G (p.Glu334=)
c.156-151A>G
c.740A>G (n.740A>G)
dbSNP
16g.67940225T>GCA396375889LCATc.1002A>C (p.Glu334Asp)
c.156-151A>C
c.740A>C (n.740A>C)
16g.67940225T=CA2229563270LCATc.1002A= (p.Glu334=)
c.156-151A=
c.740A= (n.740A=)
16g.67940226T>ACA396375890LCATc.1001A>T (p.Glu334Val)
c.156-152A>T
c.739A>T (n.739A>T)
16g.67940226T>CCA396375892LCATc.1001A>G (p.Glu334Gly)
c.156-152A>G
c.739A>G (n.739A>G)
16g.67940226T>GCA396375891LCATc.1001A>C (p.Glu334Ala)
c.156-152A>C
c.739A>C (n.739A>C)
16g.67940227C>ACA396375893LCATc.1000G>T (p.Glu334Ter)
c.156-153G>T
c.738G>T (n.738G>T)
16g.67940227C>GCA396375894LCATc.1000G>C (p.Glu334Gln)
c.156-153G>C
c.738G>C (n.738G>C)
16g.67940227C>TCA396375895LCATc.1000G>A (p.Glu334Lys)
c.156-153G>A
c.738G>A (n.738G>A)
16g.67940228C>ACA496384077LCATc.999G>T (p.Val333=)
c.156-154G>T
c.737G>T (n.737G>T)
16g.67940228C>GCA496384079LCATc.999G>C (p.Val333=)
c.156-154G>C
c.737G>C (n.737G>C)
16g.67940228C>TCA496384078LCATc.999G>A (p.Val333=)
c.156-154G>A
c.737G>A (n.737G>A)
16g.67940229A>CCA396375896LCATc.998T>G (p.Val333Gly)
c.156-155T>G
c.736T>G (n.736T>G)
16g.67940229A>GCA396375897LCATc.998T>C (p.Val333Ala)
c.156-155T>C
c.736T>C (n.736T>C)
16g.67940229A>TCA396375898LCATc.998T>A (p.Val333Glu)
c.156-155T>A
c.736T>A (n.736T>A)
16g.67940230C>ACA396375899LCATc.997G>T (p.Val333Leu)
c.156-156G>T
c.735G>T (n.735G>T)
16g.67940230C=CA2229563271LCATc.997G= (p.Val333=)
c.156-156G=
c.735G= (n.735G=)
16g.67940230C>GCA396375900LCATc.997G>C (p.Val333Leu)
c.156-156G>C
c.735G>C (n.735G>C)
16g.67940230C>TCA8120920LCATc.997G>A (p.Val333Met)
c.156-156G>A
c.735G>A (n.735G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
16g.67940231A>CCA496384080LCATc.996T>G (p.Gly332=)
c.156-157T>G
c.734T>G (n.734T>G)
16g.67940231A>GCA496384082LCATc.996T>C (p.Gly332=)
c.156-157T>C
c.734T>C (n.734T>C)
16g.67940231A>TCA496384081LCATc.996T>A (p.Gly332=)
c.156-157T>A
c.734T>A (n.734T>A)
16g.67940232C>ACA396375901LCATc.995G>T (p.Gly332Val)
c.156-158G>T
c.733G>T (n.733G>T)
16g.67940232C>GCA396375902LCATc.995G>C (p.Gly332Ala)
c.156-158G>C
c.733G>C (n.733G>C)
16g.67940232C>TCA396375903LCATc.995G>A (p.Gly332Asp)
c.156-158G>A
c.733G>A (n.733G>A)
16g.67940233C>ACA396375905LCATc.994G>T (p.Gly332Cys)
c.156-159G>T
c.732G>T (n.732G>T)
16g.67940233C=CA2229563272LCATc.994G= (p.Gly332=)
c.156-159G=
c.732G= (n.732G=)
16g.67940233C>GCA396375904LCATc.994G>C (p.Gly332Arg)
c.156-159G>C
c.732G>C (n.732G>C)
gnomAD v4
16g.67940233C>TCA283160801LCATc.994G>A (p.Gly332Ser)
c.156-159G>A
c.732G>A (n.732G>A)
dbSNP
16g.67940234A>CCA496384083LCATc.993T>G (p.Pro331=)
c.156-160T>G
c.731T>G (n.731T>G)
gnomAD v4
16g.67940234A>GCA496384084LCATc.993T>C (p.Pro331=)
c.156-160T>C
c.731T>C (n.731T>C)
gnomAD v4
16g.67940234A>TCA496384085LCATc.993T>A (p.Pro331=)
c.156-160T>A
c.731T>A (n.731T>A)
16g.67940235G>ACA396375906LCATc.992C>T (p.Pro331Leu)
c.156-161C>T
c.730C>T (n.730C>T)
dbSNP gnomAD v4
16g.67940235G>CCA396375908LCATc.992C>G (p.Pro331Arg)
c.156-161C>G
c.730C>G (n.730C>G)
16g.67940235G=CA2229563273LCATc.992C= (p.Pro331=)
c.156-161C=
c.730C= (n.730C=)
16g.67940235G>TCA396375907LCATc.992C>A (p.Pro331His)
c.156-161C>A
c.730C>A (n.730C>A)
16g.67940236G>ACA396375909LCATc.991C>T (p.Pro331Ser)
c.156-162C>T
c.729C>T (n.729C>T)
16g.67940236G>CCA396375910LCATc.991C>G (p.Pro331Ala)
c.156-162C>G
c.729C>G (n.729C>G)
16g.67940236G>TCA396375911LCATc.991C>A (p.Pro331Thr)
c.156-162C>A
c.729C>A (n.729C>A)
16g.67940236_67940247dupCA723097401LCATc.980_991dup (p.Ala330_Pro331insArgLeuProAla)
c.156-173_156-162dup
c.718_729dup (n.718_729dup)
dbSNP gnomAD v3 gnomAD v4
16g.67940237T>ACA496384086LCATc.990A>T (p.Ala330=)
c.156-163A>T
c.728A>T (n.728A>T)
16g.67940237T>CCA496384088LCATc.990A>G (p.Ala330=)
c.156-163A>G
c.728A>G (n.728A>G)
ClinVar dbSNP gnomAD v2 gnomAD v4
16g.67940237T>GCA496384087LCATc.990A>C (p.Ala330=)
c.156-163A>C
c.728A>C (n.728A>C)
16g.67940237T=CA2229563274LCATc.990A= (p.Ala330=)
c.156-163A=
c.728A= (n.728A=)
16g.67940238G>ACA396375912LCATc.989C>T (p.Ala330Val)
c.156-164C>T
c.727C>T (n.727C>T)
COSMIC
16g.67940238G>CCA396375913LCATc.989C>G (p.Ala330Gly)
c.156-164C>G
c.727C>G (n.727C>G)
16g.67940238G>TCA396375914LCATc.989C>A (p.Ala330Glu)
c.156-164C>A
c.727C>A (n.727C>A)
gnomAD v4
16g.67940239C>ACA396375915LCATc.988G>T (p.Ala330Ser)
c.156-165G>T
c.726G>T (n.726G>T)
16g.67940239C=CA2229563275LCATc.988G= (p.Ala330=)
c.156-165G=
c.726G= (n.726G=)
16g.67940239C>GCA396375916LCATc.988G>C (p.Ala330Pro)
c.156-165G>C
c.726G>C (n.726G>C)
gnomAD v4
16g.67940239C>TCA8120921LCATc.988G>A (p.Ala330Thr)
c.156-165G>A
c.726G>A (n.726G>A)
dbSNP ExAC gnomAD v2 gnomAD v4
16g.67940240T>ACA496384089LCATc.987A>T (p.Pro329=)
c.156-166A>T
c.725A>T (n.725A>T)
16g.67940240T>CCA496384090LCATc.987A>G (p.Pro329=)
c.156-166A>G
c.725A>G (n.725A>G)
16g.67940240T>GCA496384091LCATc.987A>C (p.Pro329=)
c.156-166A>C
c.725A>C (n.725A>C)
16g.67940241G>ACA396375917LCATc.986C>T (p.Pro329Leu)
c.156-167C>T
c.724C>T (n.724C>T)
dbSNP gnomAD v4
16g.67940241G>CCA396375918LCATc.986C>G (p.Pro329Arg)
c.156-167C>G
c.724C>G (n.724C>G)
16g.67940241G=CA2229563276LCATc.986C= (p.Pro329=)
c.156-167C=
c.724C= (n.724C=)
16g.67940241G>TCA396375919LCATc.986C>A (p.Pro329Gln)
c.156-167C>A
c.724C>A (n.724C>A)
16g.67940242G>ACA396375920LCATc.985C>T (p.Pro329Ser)
c.156-168C>T
c.723C>T (n.723C>T)
16g.67940242G>CCA396375922LCATc.985C>G (p.Pro329Ala)
c.156-168C>G
c.723C>G (n.723C>G)
16g.67940242G>TCA396375921LCATc.985C>A (p.Pro329Thr)
c.156-168C>A
c.723C>A (n.723C>A)
16g.67940243G>ACA283160815LCATc.984C>T (p.Leu328=)
c.156-169C>T
c.722C>T (n.722C>T)
dbSNP
16g.67940243G>CCA496384092LCATc.984C>G (p.Leu328=)
c.156-169C>G
c.722C>G (n.722C>G)
dbSNP
16g.67940243G=CA2229563277LCATc.984C= (p.Leu328=)
c.156-169C=
c.722C= (n.722C=)
16g.67940243G>TCA496384093LCATc.984C>A (p.Leu328=)
c.156-169C>A
c.722C>A (n.722C>A)
16g.67940244A>CCA396375923LCATc.983T>G (p.Leu328Arg)
c.156-170T>G
c.721T>G (n.721T>G)
16g.67940244A>GCA396375924LCATc.983T>C (p.Leu328Pro)
c.156-170T>C
c.721T>C (n.721T>C)
16g.67940244A>TCA396375925LCATc.983T>A (p.Leu328His)
c.156-170T>A
c.721T>A (n.721T>A)
16g.67940245G>ACA396375926LCATc.982C>T (p.Leu328Phe)
c.156-171C>T
c.720C>T (n.720C>T)
dbSNP gnomAD v4
16g.67940245G>CCA396375927LCATc.982C>G (p.Leu328Val)
c.156-171C>G
c.720C>G (n.720C>G)
16g.67940245G=CA2229563278LCATc.982C= (p.Leu328=)
c.156-171C=
c.720C= (n.720C=)
16g.67940245G>TCA396375928LCATc.982C>A (p.Leu328Ile)
c.156-171C>A
c.720C>A (n.720C>A)
16g.67940246T>ACA496384095LCATc.981A>T (p.Gly327=)
c.156-172A>T
c.765A>T (p.Gly255=)
c.719A>T (n.719A>T)
16g.67940246T>CCA496384094LCATc.981A>G (p.Gly327=)
c.156-172A>G
c.765A>G (p.Gly255=)
c.719A>G (n.719A>G)
16g.67940246T>GCA8120922LCATc.981A>C (p.Gly327=)
c.156-172A>C
c.765A>C (p.Gly255=)
c.719A>C (n.719A>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.67940246T=CA2229563279LCATc.981A= (p.Gly327=)
c.156-172A=
c.765A= (p.Gly255=)
c.719A= (n.719A=)
16g.67940247C>ACA8120923LCATc.980G>T (p.Gly327Val)
c.156-173G>T
c.764G>T (p.Gly255Val)
c.718G>T (n.718G>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.67940247C=CA2229563280LCATc.980G= (p.Gly327=)
c.156-173G=
c.764G= (p.Gly255=)
c.718G= (n.718G=)
16g.67940247C>GCA396375929LCATc.980G>C (p.Gly327Ala)
c.156-173G>C
c.764G>C (p.Gly255Ala)
c.718G>C (n.718G>C)
16g.67940247C>TCA396375930LCATc.980G>A (p.Gly327Glu)
c.156-173G>A
c.764G>A (p.Gly255Glu)
c.718G>A (n.718G>A)
16g.67940248C>ACA396375933LCATc.979G>T (p.Gly327Ter)
c.156-174G>T
c.763G>T (p.Gly255Ter)
c.717G>T (n.717G>T)
16g.67940248C=CA2229563281LCATc.979G= (p.Gly327=)
c.156-174G=
c.763G= (p.Gly255=)
c.717G= (n.717G=)
16g.67940248C>GCA396375932LCATc.979G>C (p.Gly327Arg)
c.156-174G>C
c.763G>C (p.Gly255Arg)
c.717G>C (n.717G>C)
dbSNP gnomAD v3 gnomAD v4
16g.67940248C>TCA396375931LCATc.979G>A (p.Gly327Arg)
c.156-174G>A
c.763G>A (p.Gly255Arg)
c.717G>A (n.717G>A)
gnomAD v4
16g.67940249T>ACA496384096LCATc.978A>T (p.Ala326=)
c.156-175A>T
c.762A>T (p.Ala254=)
c.716A>T (n.716A>T)
16g.67940249T>CCA496384097LCATc.978A>G (p.Ala326=)
c.156-175A>G
c.762A>G (p.Ala254=)
c.716A>G (n.716A>G)
dbSNP
16g.67940249T>GCA496384098LCATc.978A>C (p.Ala326=)
c.156-175A>C
c.762A>C (p.Ala254=)
c.716A>C (n.716A>C)
gnomAD v4
16g.67940249T=CA2229563282LCATc.978A= (p.Ala326=)
c.156-175A=
c.762A= (p.Ala254=)
c.716A= (n.716A=)
16g.67940250G>ACA396375936LCATc.977C>T (p.Ala326Val)
c.156-176C>T
c.761C>T (p.Ala254Val)
c.715C>T (n.715C>T)
16g.67940250G>CCA396375934LCATc.977C>G (p.Ala326Gly)
c.156-176C>G
c.761C>G (p.Ala254Gly)
c.715C>G (n.715C>G)
16g.67940250G>TCA396375935LCATc.977C>A (p.Ala326Glu)
c.156-176C>A
c.761C>A (p.Ala254Glu)
c.715C>A (n.715C>A)
16g.67940251_67940263delCA2633850947LCATc.965_977del (p.Arg322GlnfsTer?)
c.156-188_156-176del
c.749_761del (p.Arg250GlnfsTer?)
c.703_715del (n.703_715del)
gnomAD v4
16g.67940251C>ACA396375937LCATc.976G>T (p.Ala326Ser)
c.156-177G>T
c.760G>T (p.Ala254Ser)
c.714G>T (n.714G>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.67940251C=CA2229563283LCATc.976G= (p.Ala326=)
c.156-177G=
c.760G= (p.Ala254=)
c.714G= (n.714G=)
16g.67940251C>GCA396375938LCATc.976G>C (p.Ala326Pro)
c.156-177G>C
c.760G>C (p.Ala254Pro)
c.714G>C (n.714G>C)
16g.67940251C>TCA8120924LCATc.976G>A (p.Ala326Thr)
c.156-177G>A
c.760G>A (p.Ala254Thr)
c.714G>A (n.714G>A)
dbSNP ExAC gnomAD v2 gnomAD v4
16g.67940252C>ACA496384099LCATc.975G>T (p.Leu325=)
c.156-178G>T
c.759G>T (p.Leu253=)
c.713G>T (n.713G>T)
16g.67940252C>GCA496384101LCATc.975G>C (p.Leu325=)
c.156-178G>C
c.759G>C (p.Leu253=)
c.713G>C (n.713G>C)
16g.67940252C>TCA496384100LCATc.975G>A (p.Leu325=)
c.156-178G>A
c.759G>A (p.Leu253=)
c.713G>A (n.713G>A)
gnomAD v4
16g.67940252_67940255delinsCAGGCA2229563284LCATc.972_975delinsCCTG (p.Leu324=)
c.156-181_156-178delinsCCTG
c.756_759delinsCCTG (p.Leu252=)
c.710_713delinsCCTG (n.710_713delinsCCTG)
16g.67940253A=CA2229563285LCATc.974T= (p.Leu325=)
c.156-179T=
c.758T= (p.Leu253=)
c.712T= (n.712T=)
16g.67940253A>CCA396375941LCATc.974T>G (p.Leu325Arg)
c.156-179T>G
c.758T>G (p.Leu253Arg)
c.712T>G (n.712T>G)
16g.67940253A>GCA396375940LCATc.974T>C (p.Leu325Pro)
c.156-179T>C
c.758T>C (p.Leu253Pro)
c.712T>C (n.712T>C)
dbSNP gnomAD v2
16g.67940253A>TCA396375939LCATc.974T>A (p.Leu325Gln)
c.156-179T>A
c.758T>A (p.Leu253Gln)
c.712T>A (n.712T>A)
16g.67940256_67940258delCA116428LCATc.972_974del (p.Leu325del)
c.156-181_156-179del
c.756_758del (p.Leu253del)
c.710_712del (n.710_712del)
ClinVar dbSNP gnomAD v4
16g.67940254G>ACA496384102LCATc.973C>T (p.Leu325=)
c.156-180C>T
c.757C>T (p.Leu253=)
c.711C>T (n.711C>T)
COSMIC
16g.67940254G>CCA396375942LCATc.973C>G (p.Leu325Val)
c.156-180C>G
c.757C>G (p.Leu253Val)
c.711C>G (n.711C>G)
16g.67940254G>TCA396375943LCATc.973C>A (p.Leu325Met)
c.156-180C>A
c.757C>A (p.Leu253Met)
c.711C>A (n.711C>A)
16g.67940255G>ACA283160834LCATc.972C>T (p.Leu324=)
c.156-181C>T
c.756C>T (p.Leu252=)
c.710C>T (n.710C>T)
ClinVar dbSNP gnomAD v3 gnomAD v4
16g.67940255G>CCA496384103LCATc.972C>G (p.Leu324=)
c.156-181C>G
c.756C>G (p.Leu252=)
c.710C>G (n.710C>G)
16g.67940255G=CA2229563286LCATc.972C= (p.Leu324=)
c.156-181C=
c.756C= (p.Leu252=)
c.710C= (n.710C=)
16g.67940255G>TCA496384104LCATc.972C>A (p.Leu324=)
c.156-181C>A
c.756C>A (p.Leu252=)
c.710C>A (n.710C>A)
16g.67940256A>CCA396375944LCATc.971T>G (p.Leu324Arg)
c.156-182T>G
c.755T>G (p.Leu252Arg)
c.709T>G (n.709T>G)
16g.67940256A>GCA396375945LCATc.971T>C (p.Leu324Pro)
c.156-182T>C
c.755T>C (p.Leu252Pro)
c.709T>C (n.709T>C)
16g.67940256A>TCA396375946LCATc.971T>A (p.Leu324His)
c.156-182T>A
c.755T>A (p.Leu252His)
c.709T>A (n.709T>A)
dbSNP
16g.67940257G>ACA396375947LCATc.970C>T (p.Leu324Phe)
c.156-183C>T
c.754C>T (p.Leu252Phe)
c.708C>T (n.708C>T)
gnomAD v4
16g.67940257G>CCA396375949LCATc.970C>G (p.Leu324Val)
c.156-183C>G
c.754C>G (p.Leu252Val)
c.708C>G (n.708C>G)
dbSNP gnomAD v4
16g.67940257G>TCA396375948LCATc.970C>A (p.Leu324Ile)
c.156-183C>A
c.754C>A (p.Leu252Ile)
c.708C>A (n.708C>A)
COSMIC
16g.67940258G>ACA496384105LCATc.969C>T (p.Asp323=)
c.156-184C>T
c.753C>T (p.Asp251=)
c.707C>T (n.707C>T)
gnomAD v4
16g.67940258G>CCA396375950LCATc.969C>G (p.Asp323Glu)
c.156-184C>G
c.753C>G (p.Asp251Glu)
c.707C>G (n.707C>G)
16g.67940258G=CA2229563287LCATc.969C= (p.Asp323=)
c.156-184C=
c.753C= (p.Asp251=)
c.707C= (n.707C=)
16g.67940258G>TCA396375951LCATc.969C>A (p.Asp323Glu)
c.156-184C>A
c.753C>A (p.Asp251Glu)
c.707C>A (n.707C>A)
dbSNP
16g.67940259T>ACA396375952LCATc.968A>T (p.Asp323Val)
c.156-185A>T
c.752A>T (p.Asp251Val)
c.706A>T (n.706A>T)
16g.67940259T>CCA8120925LCATc.968A>G (p.Asp323Gly)
c.156-185A>G
c.752A>G (p.Asp251Gly)
c.706A>G (n.706A>G)
dbSNP ExAC
16g.67940259T>GCA396375953LCATc.968A>C (p.Asp323Ala)
c.156-185A>C
c.752A>C (p.Asp251Ala)
c.706A>C (n.706A>C)
16g.67940259T=CA2229563288LCATc.968A= (p.Asp323=)
c.156-185A=
c.752A= (p.Asp251=)
c.706A= (n.706A=)
16g.67940260C>ACA396375954LCATc.967G>T (p.Asp323Tyr)
c.156-186G>T
c.751G>T (p.Asp251Tyr)
c.705G>T (n.705G>T)
16g.67940260C>GCA396375955LCATc.967G>C (p.Asp323His)
c.156-186G>C
c.751G>C (p.Asp251His)
c.705G>C (n.705G>C)
16g.67940260C>TCA396375956LCATc.967G>A (p.Asp323Asn)
c.156-186G>A
c.751G>A (p.Asp251Asn)
c.705G>A (n.705G>A)
16g.67940261A>CCA496384108LCATc.966T>G (p.Arg322=)
c.156-187T>G
c.750T>G (p.Arg250=)
c.704T>G (n.704T>G)
16g.67940261A>GCA496384107LCATc.966T>C (p.Arg322=)
c.156-187T>C
c.750T>C (p.Arg250=)
c.704T>C (n.704T>C)
16g.67940261A>TCA496384106LCATc.966T>A (p.Arg322=)
c.156-187T>A
c.750T>A (p.Arg250=)
c.704T>A (n.704T>A)
16g.67940262C>ACA396375957LCATc.965G>T (p.Arg322Leu)
c.156-188G>T
c.749G>T (p.Arg250Leu)
c.703G>T (n.703G>T)
16g.67940262C=CA2229563289LCATc.965G= (p.Arg322=)
c.156-188G=
c.749G= (p.Arg250=)
c.703G= (n.703G=)
16g.67940262C>GCA396375958LCATc.965G>C (p.Arg322Pro)
c.156-188G>C
c.749G>C (p.Arg250Pro)
c.703G>C (n.703G>C)
16g.67940262C>TCA8120926LCATc.965G>A (p.Arg322His)
c.156-188G>A
c.749G>A (p.Arg250His)
c.703G>A (n.703G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.67940263G>ACA396375960LCATc.964C>T (p.Arg322Cys)
c.156-189C>T
c.748C>T (p.Arg250Cys)
c.702C>T (n.702C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.67940263G>CCA396375961LCATc.964C>G (p.Arg322Gly)
c.156-189C>G
c.748C>G (p.Arg250Gly)
c.702C>G (n.702C>G)
16g.67940263G=CA2229563290LCATc.964C= (p.Arg322=)
c.156-189C=
c.748C= (p.Arg250=)
c.702C= (n.702C=)
16g.67940263G>TCA396375959LCATc.964C>A (p.Arg322Ser)
c.156-189C>A
c.748C>A (p.Arg250Ser)
c.702C>A (n.702C>A)
16g.67940264T>ACA496384109LCATc.963A>T (p.Ser321=)
c.156-190A>T
c.747A>T (p.Ser249=)
c.701A>T (n.701A>T)
16g.67940264T>CCA496384110LCATc.963A>G (p.Ser321=)
c.156-190A>G
c.747A>G (p.Ser249=)
c.701A>G (n.701A>G)
16g.67940264T>GCA496384111LCATc.963A>C (p.Ser321=)
c.156-190A>C
c.747A>C (p.Ser249=)
c.701A>C (n.701A>C)
16g.67940264_67940266delCA2576033448LCATc.961_963del (p.Ser321del)
c.156-192_156-190del
c.745_747del (p.Ser249del)
c.699_701del (n.699_701del)
16g.67940265G>ACA396375962LCATc.962C>T (p.Ser321Leu)
c.156-191C>T
c.746C>T (p.Ser249Leu)
c.700C>T (n.700C>T)
COSMIC
16g.67940265G>CCA396375963LCATc.962C>G (p.Ser321Ter)
c.156-191C>G
c.746C>G (p.Ser249Ter)
c.700C>G (n.700C>G)
16g.67940265G>TCA396375964LCATc.962C>A (p.Ser321Ter)
c.156-191C>A
c.746C>A (p.Ser249Ter)
c.700C>A (n.700C>A)
16g.67940266A>CCA396375965LCATc.961T>G (p.Ser321Ala)
c.156-192T>G
c.745T>G (p.Ser249Ala)
c.699T>G (n.699T>G)
16g.67940266A>GCA396375966LCATc.961T>C (p.Ser321Pro)
c.156-192T>C
c.745T>C (p.Ser249Pro)
c.699T>C (n.699T>C)
16g.67940266A>TCA396375967LCATc.961T>A (p.Ser321Thr)
c.156-192T>A
c.745T>A (p.Ser249Thr)
c.699T>A (n.699T>A)
16g.67940267C>ACA396375968LCATc.960G>T (p.Gln320His)
c.156-193G>T
c.744G>T (p.Gln248His)
c.698G>T (n.698G>T)
16g.67940267C>GCA396375969LCATc.960G>C (p.Gln320His)
c.156-193G>C
c.744G>C (p.Gln248His)
c.698G>C (n.698G>C)
16g.67940267C>TCA496384112LCATc.960G>A (p.Gln320=)
c.156-193G>A
c.744G>A (p.Gln248=)
c.698G>A (n.698G>A)
16g.67940268T>ACA396375970LCATc.959A>T (p.Gln320Leu)
c.156-194A>T
c.743A>T (p.Gln248Leu)
c.697A>T (n.697A>T)
16g.67940268T>CCA396375971LCATc.959A>G (p.Gln320Arg)
c.156-194A>G
c.743A>G (p.Gln248Arg)
c.697A>G (n.697A>G)
16g.67940268T>GCA396375972LCATc.959A>C (p.Gln320Pro)
c.156-194A>C
c.743A>C (p.Gln248Pro)
c.697A>C (n.697A>C)
16g.67940269G>ACA396375973LCATc.958C>T (p.Gln320Ter)
c.156-195C>T
c.742C>T (p.Gln248Ter)
c.696C>T (n.696C>T)
gnomAD v4
16g.67940269G>CCA396375974LCATc.958C>G (p.Gln320Glu)
c.156-195C>G
c.742C>G (p.Gln248Glu)
c.696C>G (n.696C>G)
16g.67940269G>TCA396375975LCATc.958C>A (p.Gln320Lys)
c.156-195C>A
c.742C>A (p.Gln248Lys)
c.696C>A (n.696C>A)

Number of alleles fetched