Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.186209231A>CCA358950635CYP4V2,KLKB1c.1364A>C (p.Tyr455Ser)
n.599A>C
n.6062A>C
c.160A>C
n.454A>C
c.1361A>C (p.Tyr454Ser)
c.968A>C (p.Tyr323Ser)
4g.186209231A>GCA358950637CYP4V2,KLKB1c.1364A>G (p.Tyr455Cys)
n.599A>G
n.6062A>G
c.160A>G
n.454A>G
c.1361A>G (p.Tyr454Cys)
c.968A>G (p.Tyr323Cys)
4g.186209231A>TCA358950636CYP4V2,KLKB1c.1364A>T (p.Tyr455Phe)
n.599A>T
n.6062A>T
c.160A>T
n.454A>T
c.1361A>T (p.Tyr454Phe)
c.968A>T (p.Tyr323Phe)
 gnomAD v4
4g.186209232T>ACA358950638CYP4V2,KLKB1c.1365T>A (p.Tyr455Ter)
n.600T>A
n.6063T>A
c.161T>A
n.455T>A
c.1362T>A (p.Tyr454Ter)
c.969T>A (p.Tyr323Ter)
4g.186209232T>CCA442882849CYP4V2,KLKB1c.1365T>C (p.Tyr455=)
n.600T>C
n.6063T>C
c.161T>C
n.455T>C
c.1362T>C (p.Tyr454=)
c.969T>C (p.Tyr323=)
 dbSNP
4g.186209232T>GCA358950639CYP4V2,KLKB1c.1365T>G (p.Tyr455Ter)
n.600T>G
n.6063T>G
c.161T>G
n.455T>G
c.1362T>G (p.Tyr454Ter)
c.969T>G (p.Tyr323Ter)
4g.186209232T=CA1519891482CYP4V2,KLKB1c.1365T= (p.Tyr455=)
n.600T=
n.6063T=
c.161T=
n.455T=
c.1362T= (p.Tyr454=)
c.969T= (p.Tyr323=)
4g.186209233G>ACA358950640CYP4V2,KLKB1c.1366G>A (p.Ala456Thr)
n.601G>A
n.6064G>A
c.162G>A
n.456G>A
c.1363G>A (p.Ala455Thr)
c.970G>A (p.Ala324Thr)
4g.186209233G>CCA358950641CYP4V2,KLKB1c.1366G>C (p.Ala456Pro)
n.601G>C
n.6064G>C
c.162G>C
n.456G>C
c.1363G>C (p.Ala455Pro)
c.970G>C (p.Ala324Pro)
4g.186209233G>TCA358950642CYP4V2,KLKB1c.1366G>T (p.Ala456Ser)
n.601G>T
n.6064G>T
c.162G>T
n.456G>T
c.1363G>T (p.Ala455Ser)
c.970G>T (p.Ala324Ser)
4g.186209234C>ACA358950643CYP4V2,KLKB1c.1367C>A (p.Ala456Asp)
n.602C>A
n.6065C>A
c.163C>A
n.457C>A
c.1364C>A (p.Ala455Asp)
c.971C>A (p.Ala324Asp)
4g.186209234C=CA1519891483CYP4V2,KLKB1c.1367C= (p.Ala456=)
n.602C=
n.6065C=
c.163C=
n.457C=
c.1364C= (p.Ala455=)
c.971C= (p.Ala324=)
4g.186209234C>GCA3162842CYP4V2,KLKB1c.1367C>G (p.Ala456Gly)
n.602C>G
n.6065C>G
c.163C>G
n.457C>G
c.1364C>G (p.Ala455Gly)
c.971C>G (p.Ala324Gly)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.186209234C>TCA358950644CYP4V2,KLKB1c.1367C>T (p.Ala456Val)
n.602C>T
n.6065C>T
c.163C>T
n.457C>T
c.1364C>T (p.Ala455Val)
c.971C>T (p.Ala324Val)
4g.186209235C>ACA442882862CYP4V2,KLKB1c.1368C>A (p.Ala456=)
n.603C>A
n.6066C>A
c.164C>A
n.458C>A
c.1365C>A (p.Ala455=)
c.972C>A (p.Ala324=)
4g.186209235C>GCA442882864CYP4V2,KLKB1c.1368C>G (p.Ala456=)
n.603C>G
n.6066C>G
c.164C>G
n.458C>G
c.1365C>G (p.Ala455=)
c.972C>G (p.Ala324=)
4g.186209235C>TCA442882866CYP4V2,KLKB1c.1368C>T (p.Ala456=)
n.603C>T
n.6066C>T
c.164C>T
n.458C>T
c.1365C>T (p.Ala455=)
c.972C>T (p.Ala324=)
 ClinVar dbSNP
4g.186209236T>ACA358950645CYP4V2,KLKB1c.1369T>A (p.Tyr457Asn)
n.604T>A
n.6067T>A
c.165T>A
n.459T>A
c.1366T>A (p.Tyr456Asn)
c.973T>A (p.Tyr325Asn)
4g.186209236T>CCA358950646CYP4V2,KLKB1c.1369T>C (p.Tyr457His)
n.604T>C
n.6067T>C
c.165T>C
n.459T>C
c.1366T>C (p.Tyr456His)
c.973T>C (p.Tyr325His)
 dbSNP gnomAD v3 gnomAD v4
4g.186209236T>GCA358950647CYP4V2,KLKB1c.1369T>G (p.Tyr457Asp)
n.604T>G
n.6067T>G
c.165T>G
n.459T>G
c.1366T>G (p.Tyr456Asp)
c.973T>G (p.Tyr325Asp)
4g.186209236T=CA1519891484CYP4V2,KLKB1c.1369T= (p.Tyr457=)
n.604T=
n.6067T=
c.165T=
n.459T=
c.1366T= (p.Tyr456=)
c.973T= (p.Tyr325=)
4g.186209237A=CA1519891485CYP4V2,KLKB1c.1370A= (p.Tyr457=)
n.605A=
n.6068A=
c.166A=
n.460A=
c.1367A= (p.Tyr456=)
c.974A= (p.Tyr325=)
4g.186209237A>CCA358950649CYP4V2,KLKB1c.1370A>C (p.Tyr457Ser)
n.605A>C
n.6068A>C
c.166A>C
n.460A>C
c.1367A>C (p.Tyr456Ser)
c.974A>C (p.Tyr325Ser)
4g.186209237A>GCA3162843CYP4V2,KLKB1c.1370A>G (p.Tyr457Cys)
n.605A>G
n.6068A>G
c.166A>G
n.460A>G
c.1367A>G (p.Tyr456Cys)
c.974A>G (p.Tyr325Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.186209237A>TCA358950648CYP4V2,KLKB1c.1370A>T (p.Tyr457Phe)
n.605A>T
n.6068A>T
c.166A>T
n.460A>T
c.1367A>T (p.Tyr456Phe)
c.974A>T (p.Tyr325Phe)
 gnomAD v4
4g.186209237dupCA2672897762CYP4V2,KLKB1c.1370dup (p.Tyr457Ter)
n.605dup
n.6068dup
c.166dup
n.460dup
c.1367dup (p.Tyr456Ter)
c.974dup (p.Tyr325Ter)
 gnomAD v4
4g.186209238C>ACA358950650CYP4V2,KLKB1c.1371C>A (p.Tyr457Ter)
n.606C>A
n.6069C>A
c.167C>A
n.461C>A
c.1368C>A (p.Tyr456Ter)
c.975C>A (p.Tyr325Ter)
4g.186209238C=CA1519891486CYP4V2,KLKB1c.1371C= (p.Tyr457=)
n.606C=
n.6069C=
c.167C=
n.461C=
c.1368C= (p.Tyr456=)
c.975C= (p.Tyr325=)
4g.186209238C>GCA358950651CYP4V2,KLKB1c.1371C>G (p.Tyr457Ter)
n.606C>G
n.6069C>G
c.167C>G
n.461C>G
c.1368C>G (p.Tyr456Ter)
c.975C>G (p.Tyr325Ter)
4g.186209238C>TCA3162844CYP4V2,KLKB1c.1371C>T (p.Tyr457=)
n.606C>T
n.6069C>T
c.167C>T
n.461C>T
c.1368C>T (p.Tyr456=)
c.975C>T (p.Tyr325=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.186209239G>ACA3162845CYP4V2,KLKB1c.1372G>A (p.Val458Met)
n.607G>A
n.6070G>A
c.168G>A
n.462G>A
c.1369G>A (p.Val457Met)
c.976G>A (p.Val326Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.186209239G>CCA358950652CYP4V2,KLKB1c.1372G>C (p.Val458Leu)
n.607G>C
n.6070G>C
c.168G>C
n.462G>C
c.1369G>C (p.Val457Leu)
c.976G>C (p.Val326Leu)
4g.186209239G=CA1519891487CYP4V2,KLKB1c.1372G= (p.Val458=)
n.607G=
n.6070G=
c.168G=
n.462G=
c.1369G= (p.Val457=)
c.976G= (p.Val326=)
4g.186209239G>TCA358950653CYP4V2,KLKB1c.1372G>T (p.Val458Leu)
n.607G>T
n.6070G>T
c.168G>T
n.462G>T
c.1369G>T (p.Val457Leu)
c.976G>T (p.Val326Leu)
4g.186209240T>ACA358950654CYP4V2,KLKB1c.1373T>A (p.Val458Glu)
n.608T>A
n.6071T>A
c.169T>A
n.463T>A
c.1370T>A (p.Val457Glu)
c.977T>A (p.Val326Glu)
4g.186209240T>CCA358950655CYP4V2,KLKB1c.1373T>C (p.Val458Ala)
n.608T>C
n.6071T>C
c.169T>C
n.463T>C
c.1370T>C (p.Val457Ala)
c.977T>C (p.Val326Ala)
4g.186209240T>GCA358950656CYP4V2,KLKB1c.1373T>G (p.Val458Gly)
n.608T>G
n.6071T>G
c.169T>G
n.463T>G
c.1370T>G (p.Val457Gly)
c.977T>G (p.Val326Gly)
4g.186209241G>ACA442882889CYP4V2,KLKB1c.1374G>A (p.Val458=)
n.609G>A
n.6072G>A
c.170G>A
n.464G>A
c.1371G>A (p.Val457=)
c.978G>A (p.Val326=)
 gnomAD v4
4g.186209241G>CCA442882890CYP4V2,KLKB1c.1374G>C (p.Val458=)
n.609G>C
n.6072G>C
c.170G>C
n.464G>C
c.1371G>C (p.Val457=)
c.978G>C (p.Val326=)
4g.186209241G>TCA442882892CYP4V2,KLKB1c.1374G>T (p.Val458=)
n.609G>T
n.6072G>T
c.170G>T
n.464G>T
c.1371G>T (p.Val457=)
c.978G>T (p.Val326=)
 gnomAD v4
4g.186209242C>ACA358950657CYP4V2,KLKB1c.1375C>A (p.Pro459Thr)
n.610C>A
n.6073C>A
c.171C>A
n.465C>A
c.1372C>A (p.Pro458Thr)
c.979C>A (p.Pro327Thr)
 gnomAD v4
4g.186209242C=CA1519891488CYP4V2,KLKB1c.1375C= (p.Pro459=)
n.610C=
n.6073C=
c.171C=
n.465C=
c.1372C= (p.Pro458=)
c.979C= (p.Pro327=)
4g.186209242C>GCA358950658CYP4V2,KLKB1c.1375C>G (p.Pro459Ala)
n.610C>G
n.6073C>G
c.171C>G
n.465C>G
c.1372C>G (p.Pro458Ala)
c.979C>G (p.Pro327Ala)
4g.186209242C>TCA358950659CYP4V2,KLKB1c.1375C>T (p.Pro459Ser)
n.610C>T
n.6073C>T
c.171C>T
n.465C>T
c.1372C>T (p.Pro458Ser)
c.979C>T (p.Pro327Ser)
 ClinVar dbSNP gnomAD v4 COSMIC
4g.186209243C>ACA358950660CYP4V2,KLKB1c.1376C>A (p.Pro459His)
n.611C>A
n.6074C>A
c.172C>A
n.466C>A
c.1373C>A (p.Pro458His)
c.980C>A (p.Pro327His)
 ClinVar dbSNP
4g.186209243C=CA1519891489CYP4V2,KLKB1c.1376C= (p.Pro459=)
n.611C=
n.6074C=
c.172C=
n.466C=
c.1373C= (p.Pro458=)
c.980C= (p.Pro327=)
4g.186209243C>GCA358950661CYP4V2,KLKB1c.1376C>G (p.Pro459Arg)
n.611C>G
n.6074C>G
c.172C>G
n.466C>G
c.1373C>G (p.Pro458Arg)
c.980C>G (p.Pro327Arg)
4g.186209243C>TCA358950662CYP4V2,KLKB1c.1376C>T (p.Pro459Leu)
n.611C>T
n.6074C>T
c.172C>T
n.466C>T
c.1373C>T (p.Pro458Leu)
c.980C>T (p.Pro327Leu)
 ClinVar dbSNP gnomAD v2 gnomAD v4
4g.186209243_186209246delinsCCTTCA1519891490CYP4V2,KLKB1c.1376_1379delinsCCTT (p.Pro459=)
n.611_614delinsCCTT
n.6074_6077delinsCCTT
c.172_175delinsCCTT
n.466_469delinsCCTT
c.1373_1376delinsCCTT (p.Pro458=)
c.980_983delinsCCTT (p.Pro327=)
4g.186209244C>ACA442882902CYP4V2,KLKB1c.1377C>A (p.Pro459=)
n.612C>A
n.6075C>A
c.173C>A
n.467C>A
c.1374C>A (p.Pro458=)
c.981C>A (p.Pro327=)

Number of alleles fetched