Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.23358471G>ACA482922455SACSc.468C>T (p.Leu156=)
c.-1783C>T (p.=)
n.166C>T
c.27C>T (p.Leu9=)
c.492C>T (p.Leu164=)
c.459C>T (p.Leu153=)
COSMIC COSMIC
13g.23358471G>CCA482922456SACSc.468C>G (p.Leu156=)
c.-1783C>G (p.=)
n.166C>G
c.27C>G (p.Leu9=)
c.492C>G (p.Leu164=)
c.459C>G (p.Leu153=)
13g.23358471G>TCA482922462SACSc.468C>A (p.Leu156=)
c.-1783C>A (p.=)
n.166C>A
c.27C>A (p.Leu9=)
c.492C>A (p.Leu164=)
c.459C>A (p.Leu153=)
13g.23358472A>CCA387552174SACSc.467T>G (p.Leu156Arg)
c.-1784T>G (p.=)
n.165T>G
c.26T>G (p.Leu9Arg)
c.491T>G (p.Leu164Arg)
c.458T>G (p.Leu153Arg)
13g.23358472A>GCA387552175SACSc.467T>C (p.Leu156Pro)
c.-1784T>C (p.=)
n.165T>C
c.26T>C (p.Leu9Pro)
c.491T>C (p.Leu164Pro)
c.458T>C (p.Leu153Pro)
13g.23358472A>TCA387552176SACSc.467T>A (p.Leu156His)
c.-1784T>A (p.=)
n.165T>A
c.26T>A (p.Leu9His)
c.491T>A (p.Leu164His)
c.458T>A (p.Leu153His)
13g.23358473G>ACA387552177SACSc.466C>T (p.Leu156Phe)
c.-1785C>T (p.=)
n.164C>T
c.25C>T (p.Leu9Phe)
c.490C>T (p.Leu164Phe)
c.457C>T (p.Leu153Phe)
13g.23358473G>CCA387552178SACSc.466C>G (p.Leu156Val)
c.-1785C>G (p.=)
n.164C>G
c.25C>G (p.Leu9Val)
c.490C>G (p.Leu164Val)
c.457C>G (p.Leu153Val)
13g.23358473G=CA2078636596SACSc.466C= (p.Leu156=)
c.-1785C= (p.=)
n.164C=
c.25C= (p.Leu9=)
c.490C= (p.Leu164=)
c.457C= (p.Leu153=)
13g.23358473G>TCA6912073SACSc.466C>A (p.Leu156Ile)
c.-1785C>A (p.=)
n.164C>A
c.25C>A (p.Leu9Ile)
c.490C>A (p.Leu164Ile)
c.457C>A (p.Leu153Ile)
dbSNP ExAC gnomAD
13g.23358474A>CCA482922473SACSc.465T>G (p.Ala155=)
c.-1786T>G (p.=)
n.163T>G
c.24T>G (p.Ala8=)
c.489T>G (p.Ala163=)
c.456T>G (p.Ala152=)
13g.23358474A>GCA482922475SACSc.465T>C (p.Ala155=)
c.-1786T>C (p.=)
n.163T>C
c.24T>C (p.Ala8=)
c.489T>C (p.Ala163=)
c.456T>C (p.Ala152=)
13g.23358474A>TCA482922477SACSc.465T>A (p.Ala155=)
c.-1786T>A (p.=)
n.163T>A
c.24T>A (p.Ala8=)
c.489T>A (p.Ala163=)
c.456T>A (p.Ala152=)
13g.23358475G>ACA387552179SACSc.464C>T (p.Ala155Val)
c.-1787C>T (p.=)
n.162C>T
c.23C>T (p.Ala8Val)
c.488C>T (p.Ala163Val)
c.455C>T (p.Ala152Val)
13g.23358475G>CCA387552180SACSc.464C>G (p.Ala155Gly)
c.-1787C>G (p.=)
n.162C>G
c.23C>G (p.Ala8Gly)
c.488C>G (p.Ala163Gly)
c.455C>G (p.Ala152Gly)
13g.23358475G>TCA387552181SACSc.464C>A (p.Ala155Asp)
c.-1787C>A (p.=)
n.162C>A
c.23C>A (p.Ala8Asp)
c.488C>A (p.Ala163Asp)
c.455C>A (p.Ala152Asp)
13g.23358476C>ACA387552182SACSc.463G>T (p.Ala155Ser)
c.-1788G>T (p.=)
n.161G>T
c.22G>T (p.Ala8Ser)
c.487G>T (p.Ala163Ser)
c.454G>T (p.Ala152Ser)
13g.23358476C>GCA387552183SACSc.463G>C (p.Ala155Pro)
c.-1788G>C (p.=)
n.161G>C
c.22G>C (p.Ala8Pro)
c.487G>C (p.Ala163Pro)
c.454G>C (p.Ala152Pro)
13g.23358476C>TCA387552184SACSc.463G>A (p.Ala155Thr)
c.-1788G>A (p.=)
n.161G>A
c.22G>A (p.Ala8Thr)
c.487G>A (p.Ala163Thr)
c.454G>A (p.Ala152Thr)
13g.23358477T>ACA482922488SACSc.462A>T (p.Pro154=)
c.-1789A>T (p.=)
n.160A>T
c.21A>T (p.Pro7=)
c.486A>T (p.Pro162=)
c.453A>T (p.Pro151=)
13g.23358477T>CCA482922490SACSc.462A>G (p.Pro154=)
c.-1789A>G (p.=)
n.160A>G
c.21A>G (p.Pro7=)
c.486A>G (p.Pro162=)
c.453A>G (p.Pro151=)
13g.23358477T>GCA482922492SACSc.462A>C (p.Pro154=)
c.-1789A>C (p.=)
n.160A>C
c.21A>C (p.Pro7=)
c.486A>C (p.Pro162=)
c.453A>C (p.Pro151=)
13g.23358478G>ACA387552185SACSc.461C>T (p.Pro154Leu)
c.-1790C>T (p.=)
n.159C>T
c.20C>T (p.Pro7Leu)
c.485C>T (p.Pro162Leu)
c.452C>T (p.Pro151Leu)
13g.23358478G>CCA387552187SACSc.461C>G (p.Pro154Arg)
c.-1790C>G (p.=)
n.159C>G
c.20C>G (p.Pro7Arg)
c.485C>G (p.Pro162Arg)
c.452C>G (p.Pro151Arg)
13g.23358478G>TCA387552186SACSc.461C>A (p.Pro154Gln)
c.-1790C>A (p.=)
n.159C>A
c.20C>A (p.Pro7Gln)
c.485C>A (p.Pro162Gln)
c.452C>A (p.Pro151Gln)
13g.23358479G>ACA387552188SACSc.460C>T (p.Pro154Ser)
c.-1791C>T (p.=)
n.158C>T
c.19C>T (p.Pro7Ser)
c.484C>T (p.Pro162Ser)
c.451C>T (p.Pro151Ser)
gnomAD
13g.23358479G>CCA387552189SACSc.460C>G (p.Pro154Ala)
c.-1791C>G (p.=)
n.158C>G
c.19C>G (p.Pro7Ala)
c.484C>G (p.Pro162Ala)
c.451C>G (p.Pro151Ala)
13g.23358479G=CA2078636601SACSc.460C= (p.Pro154=)
c.-1791C= (p.=)
n.158C=
c.19C= (p.Pro7=)
c.484C= (p.Pro162=)
c.451C= (p.Pro151=)
13g.23358479G>TCA387552190SACSc.460C>A (p.Pro154Thr)
c.-1791C>A (p.=)
n.158C>A
c.19C>A (p.Pro7Thr)
c.484C>A (p.Pro162Thr)
c.451C>A (p.Pro151Thr)
13g.23358480C>ACA482922502SACSc.459G>T (p.Gly153=)
c.-1792G>T (p.=)
n.157G>T
c.18G>T (p.Gly6=)
c.483G>T (p.Gly161=)
c.450G>T (p.Gly150=)
13g.23358480C>GCA482922506SACSc.459G>C (p.Gly153=)
c.-1792G>C (p.=)
n.157G>C
c.18G>C (p.Gly6=)
c.483G>C (p.Gly161=)
c.450G>C (p.Gly150=)
13g.23358480C>TCA482922504SACSc.459G>A (p.Gly153=)
c.-1792G>A (p.=)
n.157G>A
c.18G>A (p.Gly6=)
c.483G>A (p.Gly161=)
c.450G>A (p.Gly150=)
13g.23358481C>ACA387552191SACSc.458G>T (p.Gly153Val)
c.-1793G>T (p.=)
n.156G>T
c.17G>T (p.Gly6Val)
c.482G>T (p.Gly161Val)
c.449G>T (p.Gly150Val)
13g.23358481C>GCA387552192SACSc.458G>C (p.Gly153Ala)
c.-1793G>C (p.=)
n.156G>C
c.17G>C (p.Gly6Ala)
c.482G>C (p.Gly161Ala)
c.449G>C (p.Gly150Ala)
13g.23358481C>TCA387552193SACSc.458G>A (p.Gly153Glu)
c.-1793G>A (p.=)
n.156G>A
c.17G>A (p.Gly6Glu)
c.482G>A (p.Gly161Glu)
c.449G>A (p.Gly150Glu)
13g.23358482C>ACA387552194SACSc.458-1G>T (p.=)
c.-1793-1G>T (p.=)
n.156-1G>T
c.17-1G>T (p.=)
c.482-1G>T (p.=)
c.449-1G>T (p.=)
13g.23358482C>GCA387552195SACSc.458-1G>C (p.=)
c.-1793-1G>C (p.=)
n.156-1G>C
c.17-1G>C (p.=)
c.482-1G>C (p.=)
c.449-1G>C (p.=)
13g.23358482C>TCA387552196SACSc.458-1G>A (p.=)
c.-1793-1G>A (p.=)
n.156-1G>A
c.17-1G>A (p.=)
c.482-1G>A (p.=)
c.449-1G>A (p.=)
13g.23358483T>ACA387552199SACSc.458-2A>T (p.=)
c.-1793-2A>T (p.=)
n.156-2A>T
c.17-2A>T (p.=)
c.482-2A>T (p.=)
c.449-2A>T (p.=)
13g.23358483T>CCA387552198SACSc.458-2A>G (p.=)
c.-1793-2A>G (p.=)
n.156-2A>G
c.17-2A>G (p.=)
c.482-2A>G (p.=)
c.449-2A>G (p.=)
13g.23358483T>GCA387552197SACSc.458-2A>C (p.=)
c.-1793-2A>C (p.=)
n.156-2A>C
c.17-2A>C (p.=)
c.482-2A>C (p.=)
c.449-2A>C (p.=)
13g.23358485G>CCA6912074SACSc.458-4C>G (p.=)
c.-1793-4C>G (p.=)
n.156-4C>G
c.17-4C>G (p.=)
c.482-4C>G (p.=)
c.449-4C>G (p.=)
dbSNP ExAC gnomAD
13g.23358485G=CA2078636603SACSc.458-4C= (p.=)
c.-1793-4C= (p.=)
n.156-4C=
c.17-4C= (p.=)
c.482-4C= (p.=)
c.449-4C= (p.=)
13g.23358495T>GCA696651705SACSc.458-14A>C (p.=)
c.-1793-14A>C (p.=)
n.156-14A>C
c.17-14A>C (p.=)
c.482-14A>C (p.=)
c.449-14A>C (p.=)
13g.23358495T=CA2078636606SACSc.458-14A= (p.=)
c.-1793-14A= (p.=)
n.156-14A=
c.17-14A= (p.=)
c.482-14A= (p.=)
c.449-14A= (p.=)
13g.23358496G>ACA6912075SACSc.458-15C>T (p.=)
c.-1793-15C>T (p.=)
n.156-15C>T
c.17-15C>T (p.=)
c.482-15C>T (p.=)
c.449-15C>T (p.=)
dbSNP ExAC gnomAD
13g.23358496G=CA2078636608SACSc.458-15C= (p.=)
c.-1793-15C= (p.=)
n.156-15C=
c.17-15C= (p.=)
c.482-15C= (p.=)
c.449-15C= (p.=)
13g.23358497C=CA2078636612SACSc.458-16G= (p.=)
c.-1793-16G= (p.=)
n.156-16G=
c.17-16G= (p.=)
c.482-16G= (p.=)
c.449-16G= (p.=)
13g.23358497C>TCA6912076SACSc.458-16G>A (p.=)
c.-1793-16G>A (p.=)
n.156-16G>A
c.17-16G>A (p.=)
c.482-16G>A (p.=)
c.449-16G>A (p.=)
dbSNP ExAC gnomAD COSMIC
13g.23358498G>ACA6912077SACSc.458-17C>T (p.=)
c.-1793-17C>T (p.=)
n.156-17C>T
c.17-17C>T (p.=)
c.482-17C>T (p.=)
c.449-17C>T (p.=)
dbSNP ExAC gnomAD

Number of alleles fetched