Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.67940121_67940123delCA623122337LCATc.1107_1109del (p.Asp370del)
c.156-46_156-44del
c.845_847del (n.845_847del)
dbSNP gnomAD v2 gnomAD v4
16g.67940121T>ACA396375673LCATc.1106A>T (p.Asp369Val)
c.156-47A>T
c.844A>T (n.844A>T)
16g.67940121T>CCA396375674LCATc.1106A>G (p.Asp369Gly)
c.156-47A>G
c.844A>G (n.844A>G)
gnomAD v4
16g.67940121T>GCA396375675LCATc.1106A>C (p.Asp369Ala)
c.156-47A>C
c.844A>C (n.844A>C)
16g.67940121_67940124delinsTCACCA2229563218LCATc.1103_1106delinsGTGA (p.Gly368=)
c.156-50_156-47delinsGTGA
c.841_844delinsGTGA (n.841_844delinsGTGA)
16g.67940122C>ACA396375676LCATc.1105G>T (p.Asp369Tyr)
c.156-48G>T
c.843G>T (n.843G>T)
16g.67940122C>GCA396375677LCATc.1105G>C (p.Asp369His)
c.156-48G>C
c.843G>C (n.843G>C)
16g.67940122C>TCA396375678LCATc.1105G>A (p.Asp369Asn)
c.156-48G>A
c.843G>A (n.843G>A)
gnomAD v4
16g.67940124_67940126delCA8120891LCATc.1103_1105del (p.Gly368del)
c.156-50_156-48del
c.841_843del (n.841_843del)
dbSNP ExAC gnomAD v2 gnomAD v4
16g.67940123A>CCA496383877LCATc.1104T>G (p.Gly368=)
c.156-49T>G
c.842T>G (n.842T>G)
16g.67940123A>GCA496383876LCATc.1104T>C (p.Gly368=)
c.156-49T>C
c.842T>C (n.842T>C)
dbSNP gnomAD v4
16g.67940123A>TCA496383875LCATc.1104T>A (p.Gly368=)
c.156-49T>A
c.842T>A (n.842T>A)
16g.67940124C>ACA8120892LCATc.1103G>T (p.Gly368Val)
c.156-50G>T
c.841G>T (n.841G>T)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.67940124C=CA2229563219LCATc.1103G= (p.Gly368=)
c.156-50G=
c.841G= (n.841G=)
16g.67940124C>GCA396375679LCATc.1103G>C (p.Gly368Ala)
c.156-50G>C
c.841G>C (n.841G>C)
16g.67940124C>TCA396375680LCATc.1103G>A (p.Gly368Asp)
c.156-50G>A
c.841G>A (n.841G>A)
16g.67940125C>ACA396375681LCATc.1102G>T (p.Gly368Cys)
c.156-51G>T
c.840G>T (n.840G>T)
16g.67940125C=CA2229563220LCATc.1102G= (p.Gly368=)
c.156-51G=
c.840G= (n.840G=)
16g.67940125C>GCA396375682LCATc.1102G>C (p.Gly368Arg)
c.156-51G>C
c.840G>C (n.840G>C)
16g.67940125C>TCA8120893LCATc.1102G>A (p.Gly368Ser)
c.156-51G>A
c.840G>A (n.840G>A)
dbSNP ExAC gnomAD v4
16g.67940126A=CA2229563221LCATc.1101T= (p.Asp367=)
c.156-52T=
c.839T= (n.839T=)
16g.67940126A>CCA396375683LCATc.1101T>G (p.Asp367Glu)
c.156-52T>G
c.839T>G (n.839T>G)
16g.67940126A>GCA8120894LCATc.1101T>C (p.Asp367=)
c.156-52T>C
c.839T>C (n.839T>C)
dbSNP ExAC gnomAD v2 gnomAD v4
16g.67940126A>TCA396375684LCATc.1101T>A (p.Asp367Glu)
c.156-52T>A
c.839T>A (n.839T>A)
16g.67940127T>ACA396375685LCATc.1100A>T (p.Asp367Val)
c.156-53A>T
c.838A>T (n.838A>T)
16g.67940127T>CCA396375686LCATc.1100A>G (p.Asp367Gly)
c.156-53A>G
c.838A>G (n.838A>G)
16g.67940127T>GCA396375687LCATc.1100A>C (p.Asp367Ala)
c.156-53A>C
c.838A>C (n.838A>C)
16g.67940128C>ACA396375688LCATc.1099G>T (p.Asp367Tyr)
c.156-54G>T
c.837G>T (n.837G>T)
16g.67940128C>GCA396375689LCATc.1099G>C (p.Asp367His)
c.156-54G>C
c.837G>C (n.837G>C)
COSMIC
16g.67940128C>TCA396375690LCATc.1099G>A (p.Asp367Asn)
c.156-54G>A
c.837G>A (n.837G>A)
gnomAD v4
16g.67940129C>ACA396375691LCATc.1098G>T (p.Glu366Asp)
c.156-55G>T
c.836G>T (n.836G>T)
16g.67940129C=CA2229563222LCATc.1098G= (p.Glu366=)
c.156-55G=
c.836G= (n.836G=)
16g.67940129C>GCA396375692LCATc.1098G>C (p.Glu366Asp)
c.156-55G>C
c.836G>C (n.836G>C)
16g.67940129C>TCA496383884LCATc.1098G>A (p.Glu366=)
c.156-55G>A
c.836G>A (n.836G>A)
ClinVar dbSNP
16g.67940130T>ACA396375693LCATc.1097A>T (p.Glu366Val)
c.156-56A>T
c.835A>T (n.835A>T)
16g.67940130T>CCA396375694LCATc.1097A>G (p.Glu366Gly)
c.156-56A>G
c.835A>G (n.835A>G)
gnomAD v4
16g.67940130T>GCA396375695LCATc.1097A>C (p.Glu366Ala)
c.156-56A>C
c.835A>C (n.835A>C)
16g.67940131C>ACA396375697LCATc.1096G>T (p.Glu366Ter)
c.156-57G>T
c.834G>T (n.834G>T)
16g.67940131C=CA2229563223LCATc.1096G= (p.Glu366=)
c.156-57G=
c.834G= (n.834G=)
16g.67940131C>GCA396375696LCATc.1096G>C (p.Glu366Gln)
c.156-57G>C
c.834G>C (n.834G>C)
16g.67940131C>TCA8120895LCATc.1096G>A (p.Glu366Lys)
c.156-57G>A
c.834G>A (n.834G>A)
dbSNP ExAC gnomAD v2 gnomAD v4
16g.67940132A=CA2229563224LCATc.1095T= (p.Tyr365=)
c.156-58T=
c.833T= (n.833T=)
16g.67940132A>CCA396375698LCATc.1095T>G (p.Tyr365Ter)
c.156-58T>G
c.833T>G (n.833T>G)
16g.67940132A>GCA496383888LCATc.1095T>C (p.Tyr365=)
c.156-58T>C
c.833T>C (n.833T>C)
dbSNP
16g.67940132A>TCA396375699LCATc.1095T>A (p.Tyr365Ter)
c.156-58T>A
c.833T>A (n.833T>A)
16g.67940133delCA2576033439LCATc.1094del (p.Tyr365LeufsTer?)
c.156-59del
c.832del (n.832del)
16g.67940133T>ACA396375700LCATc.1094A>T (p.Tyr365Phe)
c.156-59A>T
c.832A>T (n.832A>T)
16g.67940133T>CCA396375701LCATc.1094A>G (p.Tyr365Cys)
c.156-59A>G
c.832A>G (n.832A>G)
dbSNP gnomAD v3 gnomAD v4
16g.67940133T>GCA396375702LCATc.1094A>C (p.Tyr365Ser)
c.156-59A>C
c.832A>C (n.832A>C)
16g.67940133T=CA2229563225LCATc.1094A= (p.Tyr365=)
c.156-59A=
c.832A= (n.832A=)
16g.67940134A=CA2229563226LCATc.1093T= (p.Tyr365=)
c.156-60T=
c.831T= (n.831T=)
16g.67940134A>CCA396375703LCATc.1093T>G (p.Tyr365Asp)
c.156-60T>G
c.831T>G (n.831T>G)
16g.67940134A>GCA8120896LCATc.1093T>C (p.Tyr365His)
c.156-60T>C
c.831T>C (n.831T>C)
dbSNP ExAC gnomAD v4
16g.67940134A>TCA396375704LCATc.1093T>A (p.Tyr365Asn)
c.156-60T>A
c.831T>A (n.831T>A)
16g.67940135G>ACA496383891LCATc.1092C>T (p.Leu364=)
c.156-61C>T
c.830C>T (n.830C>T)
16g.67940135G>CCA496383892LCATc.1092C>G (p.Leu364=)
c.156-61C>G
c.830C>G (n.830C>G)
16g.67940135G>TCA496383893LCATc.1092C>A (p.Leu364=)
c.156-61C>A
c.830C>A (n.830C>A)
16g.67940136A>CCA396375705LCATc.1091T>G (p.Leu364Arg)
c.156-62T>G
c.829T>G (n.829T>G)
16g.67940136A>GCA396375706LCATc.1091T>C (p.Leu364Pro)
c.156-62T>C
c.829T>C (n.829T>C)
16g.67940136A>TCA396375707LCATc.1091T>A (p.Leu364His)
c.156-62T>A
c.829T>A (n.829T>A)
16g.67940137G>ACA396375709LCATc.1090C>T (p.Leu364Phe)
c.156-63C>T
c.828C>T (n.828C>T)
gnomAD v4
16g.67940137G>CCA396375710LCATc.1090C>G (p.Leu364Val)
c.156-63C>G
c.828C>G (n.828C>G)
16g.67940137G>TCA396375708LCATc.1090C>A (p.Leu364Ile)
c.156-63C>A
c.828C>A (n.828C>A)
16g.67940138C>ACA496383896LCATc.1089G>T (p.Val363=)
c.156-64G>T
c.827G>T (n.827G>T)
16g.67940138C>GCA496383897LCATc.1089G>C (p.Val363=)
c.156-64G>C
c.827G>C (n.827G>C)
gnomAD v4
16g.67940138C>TCA496383898LCATc.1089G>A (p.Val363=)
c.156-64G>A
c.827G>A (n.827G>A)
16g.67940139A>CCA396375711LCATc.1088T>G (p.Val363Gly)
c.156-65T>G
c.826T>G (n.826T>G)
16g.67940139A>GCA396375712LCATc.1088T>C (p.Val363Ala)
c.156-65T>C
c.826T>C (n.826T>C)
16g.67940139A>TCA396375713LCATc.1088T>A (p.Val363Glu)
c.156-65T>A
c.826T>A (n.826T>A)
ClinVar
16g.67940140C>ACA396375714LCATc.1087G>T (p.Val363Leu)
c.156-66G>T
c.825G>T (n.825G>T)
16g.67940140C>GCA396375715LCATc.1087G>C (p.Val363Leu)
c.156-66G>C
c.825G>C (n.825G>C)
16g.67940140C>TCA396375716LCATc.1087G>A (p.Val363Met)
c.156-66G>A
c.825G>A (n.825G>A)
16g.67940141A=CA2229563227LCATc.1086T= (p.Gly362=)
c.156-67T=
c.824T= (n.824T=)
16g.67940141A>CCA496383902LCATc.1086T>G (p.Gly362=)
c.156-67T>G
c.824T>G (n.824T>G)
dbSNP
16g.67940141A>GCA496383903LCATc.1086T>C (p.Gly362=)
c.156-67T>C
c.824T>C (n.824T>C)
16g.67940141A>TCA496383904LCATc.1086T>A (p.Gly362=)
c.156-67T>A
c.824T>A (n.824T>A)
16g.67940142C>ACA396375717LCATc.1085G>T (p.Gly362Val)
c.156-68G>T
c.823G>T (n.823G>T)
dbSNP
16g.67940142C=CA2229563228LCATc.1085G= (p.Gly362=)
c.156-68G=
c.823G= (n.823G=)
16g.67940142C>GCA8120897LCATc.1085G>C (p.Gly362Ala)
c.156-68G>C
c.823G>C (n.823G>C)
dbSNP ExAC gnomAD v2 gnomAD v4
16g.67940142C>TCA396375718LCATc.1085G>A (p.Gly362Asp)
c.156-68G>A
c.823G>A (n.823G>A)
ClinVar dbSNP
16g.67940143C>ACA396375719LCATc.1084G>T (p.Gly362Cys)
c.156-69G>T
c.822G>T (n.822G>T)
16g.67940143C>GCA396375720LCATc.1084G>C (p.Gly362Arg)
c.156-69G>C
c.822G>C (n.822G>C)
16g.67940143C>TCA396375721LCATc.1084G>A (p.Gly362Ser)
c.156-69G>A
c.822G>A (n.822G>A)
ClinVar
16g.67940144C>ACA496383910LCATc.1083G>T (p.Val361=)
c.156-70G>T
c.821G>T (n.821G>T)
16g.67940144C=CA2229563229LCATc.1083G= (p.Val361=)
c.156-70G=
c.821G= (n.821G=)
16g.67940144C>GCA496383908LCATc.1083G>C (p.Val361=)
c.156-70G>C
c.821G>C (n.821G>C)
16g.67940144C>TCA496383909LCATc.1083G>A (p.Val361=)
c.156-70G>A
c.821G>A (n.821G>A)
ClinVar dbSNP
16g.67940145A>CCA396375723LCATc.1082T>G (p.Val361Gly)
c.156-71T>G
c.820T>G (n.820T>G)
16g.67940145A>GCA396375724LCATc.1082T>C (p.Val361Ala)
c.156-71T>C
c.820T>C (n.820T>C)
16g.67940145A>TCA396375722LCATc.1082T>A (p.Val361Glu)
c.156-71T>A
c.820T>A (n.820T>A)
16g.67940146C>ACA396375725LCATc.1081G>T (p.Val361Leu)
c.156-72G>T
c.819G>T (n.819G>T)
16g.67940146C>GCA396375726LCATc.1081G>C (p.Val361Leu)
c.156-72G>C
c.819G>C (n.819G>C)
gnomAD v4
16g.67940146C>TCA396375727LCATc.1081G>A (p.Val361Met)
c.156-72G>A
c.819G>A (n.819G>A)
gnomAD v4
16g.67940147A>CCA496383914LCATc.1080T>G (p.Pro360=)
c.156-73T>G
c.818T>G (n.818T>G)
gnomAD v4
16g.67940147A>GCA496383915LCATc.1080T>C (p.Pro360=)
c.156-73T>C
c.818T>C (n.818T>C)
gnomAD v4
16g.67940147A>TCA496383916LCATc.1080T>A (p.Pro360=)
c.156-73T>A
c.818T>A (n.818T>A)
16g.67940148G>ACA396375728LCATc.1079C>T (p.Pro360Leu)
c.156-74C>T
c.817C>T (n.817C>T)
16g.67940148G>CCA396375729LCATc.1079C>G (p.Pro360Arg)
c.156-74C>G
c.817C>G (n.817C>G)
16g.67940148G>TCA396375730LCATc.1079C>A (p.Pro360His)
c.156-74C>A
c.817C>A (n.817C>A)
16g.67940150delCA2633850746LCATc.1079del (p.Pro360LeufsTer?)
c.156-74del
c.817del (n.817del)
gnomAD v4
16g.67940149G>ACA396375732LCATc.1078C>T (p.Pro360Ser)
c.156-75C>T
c.816C>T (n.816C>T)
16g.67940149G>CCA396375731LCATc.1078C>G (p.Pro360Ala)
c.156-75C>G
c.816C>G (n.816C>G)
16g.67940149G=CA2229563230LCATc.1078C= (p.Pro360=)
c.156-75C=
c.816C= (n.816C=)
16g.67940149G>TCA8120898LCATc.1078C>A (p.Pro360Thr)
c.156-75C>A
c.816C>A (n.816C>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.67940150G>ACA496383919LCATc.1077C>T (p.Asp359=)
c.156-76C>T
c.815C>T (n.815C>T)
ClinVar
16g.67940150G>CCA396375733LCATc.1077C>G (p.Asp359Glu)
c.156-76C>G
c.815C>G (n.815C>G)
16g.67940150G>TCA396375734LCATc.1077C>A (p.Asp359Glu)
c.156-76C>A
c.815C>A (n.815C>A)
16g.67940151T>ACA396375735LCATc.1076A>T (p.Asp359Val)
c.156-77A>T
c.814A>T (n.814A>T)
16g.67940151T>CCA396375736LCATc.1076A>G (p.Asp359Gly)
c.156-77A>G
c.814A>G (n.814A>G)
16g.67940151T>GCA396375737LCATc.1076A>C (p.Asp359Ala)
c.156-77A>C
c.814A>C (n.814A>C)
16g.67940152C>ACA396375738LCATc.1075G>T (p.Asp359Tyr)
c.156-78G>T
c.813G>T (n.813G>T)
16g.67940152C>GCA396375740LCATc.1075G>C (p.Asp359His)
c.156-78G>C
c.813G>C (n.813G>C)
16g.67940152C>TCA396375739LCATc.1075G>A (p.Asp359Asn)
c.156-78G>A
c.813G>A (n.813G>A)
16g.67940153C>ACA496383921LCATc.1074G>T (p.Thr358=)
c.156-79G>T
c.812G>T (n.812G>T)
16g.67940153C=CA2229563231LCATc.1074G= (p.Thr358=)
c.156-79G=
c.812G= (n.812G=)
16g.67940153C>GCA496383922LCATc.1074G>C (p.Thr358=)
c.156-79G>C
c.812G>C (n.812G>C)
gnomAD v4
16g.67940153C>TCA8120899LCATc.1074G>A (p.Thr358=)
c.156-79G>A
c.812G>A (n.812G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.67940154G>ACA8120900LCATc.1073C>T (p.Thr358Met)
c.156-80C>T
c.811C>T (n.811C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.67940154G>CCA396375741LCATc.1073C>G (p.Thr358Arg)
c.156-80C>G
c.811C>G (n.811C>G)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.67940154G=CA2229563232LCATc.1073C= (p.Thr358=)
c.156-80C=
c.811C= (n.811C=)
16g.67940154G>TCA396375742LCATc.1073C>A (p.Thr358Lys)
c.156-80C>A
c.811C>A (n.811C>A)
16g.67940155T>ACA396375743LCATc.1072A>T (p.Thr358Ser)
c.156-81A>T
c.810A>T (n.810A>T)
16g.67940155T>CCA396375744LCATc.1072A>G (p.Thr358Ala)
c.156-81A>G
c.810A>G (n.810A>G)
dbSNP
16g.67940155T>GCA396375745LCATc.1072A>C (p.Thr358Pro)
c.156-81A>C
c.810A>C (n.810A>C)
16g.67940155T=CA2229563233LCATc.1072A= (p.Thr358=)
c.156-81A=
c.810A= (n.810A=)
16g.67940156G>ACA283160616LCATc.1071C>T (p.Tyr357=)
c.156-82C>T
c.809C>T (n.809C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.67940156G>CCA396375746LCATc.1071C>G (p.Tyr357Ter)
c.156-82C>G
c.809C>G (n.809C>G)
16g.67940156G=CA2229563234LCATc.1071C= (p.Tyr357=)
c.156-82C=
c.809C= (n.809C=)
16g.67940156G>TCA396375747LCATc.1071C>A (p.Tyr357Ter)
c.156-82C>A
c.809C>A (n.809C>A)
16g.67940157T>ACA396375748LCATc.1070A>T (p.Tyr357Phe)
c.156-83A>T
c.808A>T (n.808A>T)
gnomAD v4
16g.67940157T>CCA396375749LCATc.1070A>G (p.Tyr357Cys)
c.156-83A>G
c.808A>G (n.808A>G)
16g.67940157T>GCA396375750LCATc.1070A>C (p.Tyr357Ser)
c.156-83A>C
c.808A>C (n.808A>C)
16g.67940158A>CCA396375751LCATc.1069T>G (p.Tyr357Asp)
c.156-84T>G
c.807T>G (n.807T>G)
16g.67940158A>GCA396375752LCATc.1069T>C (p.Tyr357His)
c.156-84T>C
c.807T>C (n.807T>C)
16g.67940158A>TCA396375753LCATc.1069T>A (p.Tyr357Asn)
c.156-84T>A
c.807T>A (n.807T>A)
16g.67940159G>ACA283160630LCATc.1068C>T (p.Pro356=)
c.156-85C>T
c.806C>T (n.806C>T)
ClinVar dbSNP gnomAD v4
16g.67940159G>CCA496383930LCATc.1068C>G (p.Pro356=)
c.156-85C>G
c.806C>G (n.806C>G)
16g.67940159G=CA2229563235LCATc.1068C= (p.Pro356=)
c.156-85C=
c.806C= (n.806C=)
16g.67940159G>TCA496383931LCATc.1068C>A (p.Pro356=)
c.156-85C>A
c.806C>A (n.806C>A)
16g.67940160G>ACA396375754LCATc.1067C>T (p.Pro356Leu)
c.156-86C>T
c.805C>T (n.805C>T)
dbSNP
16g.67940160G>CCA396375755LCATc.1067C>G (p.Pro356Arg)
c.156-86C>G
c.805C>G (n.805C>G)
16g.67940160G=CA2229563236LCATc.1067C= (p.Pro356=)
c.156-86C=
c.805C= (n.805C=)
16g.67940160G>TCA396375756LCATc.1067C>A (p.Pro356His)
c.156-86C>A
c.805C>A (n.805C>A)
16g.67940161G>ACA8120901LCATc.1066C>T (p.Pro356Ser)
c.156-87C>T
c.804C>T (n.804C>T)
dbSNP ExAC gnomAD v2 gnomAD v4
16g.67940161G>CCA396375757LCATc.1066C>G (p.Pro356Ala)
c.156-87C>G
c.804C>G (n.804C>G)
16g.67940161G=CA2229563237LCATc.1066C= (p.Pro356=)
c.156-87C=
c.804C= (n.804C=)
16g.67940161G>TCA396375758LCATc.1066C>A (p.Pro356Thr)
c.156-87C>A
c.804C>A (n.804C>A)
16g.67940162G>ACA496383933LCATc.1065C>T (p.Phe355=)
c.156-88C>T
c.803C>T (n.803C>T)
16g.67940162G>CCA396375759LCATc.1065C>G (p.Phe355Leu)
c.156-88C>G
c.803C>G (n.803C>G)
16g.67940162G>TCA396375760LCATc.1065C>A (p.Phe355Leu)
c.156-88C>A
c.803C>A (n.803C>A)
16g.67940163A=CA2229563238LCATc.1064T= (p.Phe355=)
c.156-89T=
c.802T= (n.802T=)
16g.67940163A>CCA396375761LCATc.1064T>G (p.Phe355Cys)
c.156-89T>G
c.802T>G (n.802T>G)
dbSNP gnomAD v3 gnomAD v4
16g.67940163A>GCA396375762LCATc.1064T>C (p.Phe355Ser)
c.156-89T>C
c.802T>C (n.802T>C)
16g.67940163A>TCA396375763LCATc.1064T>A (p.Phe355Tyr)
c.156-89T>A
c.802T>A (n.802T>A)
16g.67940164A>CCA396375764LCATc.1063T>G (p.Phe355Val)
c.156-90T>G
c.801T>G (n.801T>G)
16g.67940164A>GCA396375765LCATc.1063T>C (p.Phe355Leu)
c.156-90T>C
c.801T>C (n.801T>C)
16g.67940164A>TCA396375766LCATc.1063T>A (p.Phe355Ile)
c.156-90T>A
c.801T>A (n.801T>A)
16g.67940165G>ACA496383936LCATc.1062C>T (p.Gly354=)
c.156-91C>T
c.800C>T (n.800C>T)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.67940165G>CCA496383938LCATc.1062C>G (p.Gly354=)
c.156-91C>G
c.800C>G (n.800C>G)
16g.67940165G=CA2229563239LCATc.1062C= (p.Gly354=)
c.156-91C=
c.800C= (n.800C=)
16g.67940165G>TCA496383939LCATc.1062C>A (p.Gly354=)
c.156-91C>A
c.800C>A (n.800C>A)
16g.67940166C>ACA396375769LCATc.1061G>T (p.Gly354Val)
c.156-92G>T
c.799G>T (n.799G>T)
16g.67940166C>GCA396375767LCATc.1061G>C (p.Gly354Ala)
c.156-92G>C
c.799G>C (n.799G>C)
16g.67940166C>TCA396375768LCATc.1061G>A (p.Gly354Asp)
c.156-92G>A
c.799G>A (n.799G>A)
16g.67940167C>ACA396375770LCATc.1060G>T (p.Gly354Cys)
c.156-93G>T
c.798G>T (n.798G>T)
16g.67940167C=CA2229563240LCATc.1060G= (p.Gly354=)
c.156-93G=
c.798G= (n.798G=)
16g.67940167C>GCA396375771LCATc.1060G>C (p.Gly354Arg)
c.156-93G>C
c.798G>C (n.798G>C)
16g.67940167C>TCA8120902LCATc.1060G>A (p.Gly354Ser)
c.156-93G>A
c.798G>A (n.798G>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.67940168G>ACA496383943LCATc.1059C>T (p.His353=)
c.156-94C>T
c.797C>T (n.797C>T)
dbSNP gnomAD v2 gnomAD v4
16g.67940168G>CCA396375772LCATc.1059C>G (p.His353Gln)
c.156-94C>G
c.797C>G (n.797C>G)
16g.67940168G=CA2229563241LCATc.1059C= (p.His353=)
c.156-94C=
c.797C= (n.797C=)
16g.67940168G>TCA396375773LCATc.1059C>A (p.His353Gln)
c.156-94C>A
c.797C>A (n.797C>A)
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)

Number of alleles fetched