Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.48587279C>ACA406708711SULT2B1c.265C>A (p.Pro89Thr)
c.220C>A (p.Pro74Thr)
gnomAD v4 COSMIC COSMIC
19g.48587279C=CA2339970787SULT2B1c.265C= (p.Pro89=)
c.220C= (p.Pro74=)
19g.48587279C>GCA406708714SULT2B1c.265C>G (p.Pro89Ala)
c.220C>G (p.Pro74Ala)
gnomAD v4
19g.48587279C>TCA406708710SULT2B1c.265C>T (p.Pro89Ser)
c.220C>T (p.Pro74Ser)
dbSNP gnomAD v2 gnomAD v4
19g.48587280C>ACA406708720SULT2B1c.266C>A (p.Pro89Gln)
c.221C>A (p.Pro74Gln)
19g.48587280C=CA2339970788SULT2B1c.266C= (p.Pro89=)
c.221C= (p.Pro74=)
19g.48587280C>GCA406708716SULT2B1c.266C>G (p.Pro89Arg)
c.221C>G (p.Pro74Arg)
dbSNP
19g.48587280C>TCA406708718SULT2B1c.266C>T (p.Pro89Leu)
c.221C>T (p.Pro74Leu)
19g.48587281A>CCA508042628SULT2B1c.267A>C (p.Pro89=)
c.222A>C (p.Pro74=)
19g.48587281A>GCA508042630SULT2B1c.267A>G (p.Pro89=)
c.222A>G (p.Pro74=)
dbSNP
19g.48587281A>TCA508042631SULT2B1c.267A>T (p.Pro89=)
c.222A>T (p.Pro74=)
19g.48587282T>ACA406708721SULT2B1c.268T>A (p.Ser90Thr)
c.223T>A (p.Ser75Thr)
19g.48587282T>CCA406708722SULT2B1c.268T>C (p.Ser90Pro)
c.223T>C (p.Ser75Pro)
19g.48587282T>GCA406708724SULT2B1c.268T>G (p.Ser90Ala)
c.223T>G (p.Ser75Ala)
dbSNP
19g.48587282T=CA2339970789SULT2B1c.268T= (p.Ser90=)
c.223T= (p.Ser75=)
19g.48587283C>ACA406708726SULT2B1c.269C>A (p.Ser90Tyr)
c.224C>A (p.Ser75Tyr)
19g.48587283C>GCA406708728SULT2B1c.269C>G (p.Ser90Cys)
c.224C>G (p.Ser75Cys)
19g.48587283C>TCA406708730SULT2B1c.269C>T (p.Ser90Phe)
c.224C>T (p.Ser75Phe)
gnomAD v4
19g.48587284C>ACA508042634SULT2B1c.270C>A (p.Ser90=)
c.225C>A (p.Ser75=)
19g.48587284C>GCA508042636SULT2B1c.270C>G (p.Ser90=)
c.225C>G (p.Ser75=)
19g.48587284C>TCA508042637SULT2B1c.270C>T (p.Ser90=)
c.225C>T (p.Ser75=)
19g.48587285T>ACA406708732SULT2B1c.271T>A (p.Trp91Arg)
c.226T>A (p.Trp76Arg)
19g.48587285T>CCA406708734SULT2B1c.271T>C (p.Trp91Arg)
c.226T>C (p.Trp76Arg)
19g.48587285T>GCA406708736SULT2B1c.271T>G (p.Trp91Gly)
c.226T>G (p.Trp76Gly)
19g.48587286G>ACA406708741SULT2B1c.272G>A (p.Trp91Ter)
c.227G>A (p.Trp76Ter)
19g.48587286G>CCA406708739SULT2B1c.272G>C (p.Trp91Ser)
c.227G>C (p.Trp76Ser)
dbSNP gnomAD v2 gnomAD v4
19g.48587286G=CA2339970790SULT2B1c.272G= (p.Trp91=)
c.227G= (p.Trp76=)
19g.48587286G>TCA9553036SULT2B1c.272G>T (p.Trp91Leu)
c.227G>T (p.Trp76Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.48587287G>ACA406708743SULT2B1c.273G>A (p.Trp91Ter)
c.228G>A (p.Trp76Ter)
19g.48587287G>CCA406708744SULT2B1c.273G>C (p.Trp91Cys)
c.228G>C (p.Trp76Cys)
19g.48587287G>TCA406708746SULT2B1c.273G>T (p.Trp91Cys)
c.228G>T (p.Trp76Cys)
19g.48587288A>CCA406708749SULT2B1c.274A>C (p.Ile92Leu)
c.229A>C (p.Ile77Leu)
19g.48587288A>GCA406708750SULT2B1c.274A>G (p.Ile92Val)
c.229A>G (p.Ile77Val)
19g.48587288A>TCA406708751SULT2B1c.274A>T (p.Ile92Phe)
c.229A>T (p.Ile77Phe)
19g.48587289T>ACA406708753SULT2B1c.275T>A (p.Ile92Asn)
c.230T>A (p.Ile77Asn)
19g.48587289T>CCA406708754SULT2B1c.275T>C (p.Ile92Thr)
c.230T>C (p.Ile77Thr)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.48587289T>GCA406708756SULT2B1c.275T>G (p.Ile92Ser)
c.230T>G (p.Ile77Ser)
19g.48587289T=CA2339970791SULT2B1c.275T= (p.Ile92=)
c.230T= (p.Ile77=)
19g.48587290C>ACA508042641SULT2B1c.276C>A (p.Ile92=)
c.231C>A (p.Ile77=)
19g.48587290C>GCA406708759SULT2B1c.276C>G (p.Ile92Met)
c.231C>G (p.Ile77Met)
19g.48587290C>TCA508042643SULT2B1c.276C>T (p.Ile92=)
c.231C>T (p.Ile77=)
19g.48587291C>ACA406708761SULT2B1c.277C>A (p.Arg93Ser)
c.232C>A (p.Arg78Ser)
19g.48587291C=CA2339970792SULT2B1c.277C= (p.Arg93=)
c.232C= (p.Arg78=)
19g.48587291C>GCA406708763SULT2B1c.277C>G (p.Arg93Gly)
c.232C>G (p.Arg78Gly)
19g.48587291C>TCA9553037SULT2B1c.277C>T (p.Arg93Cys)
c.232C>T (p.Arg78Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
19g.48587292G>ACA9553038SULT2B1c.278G>A (p.Arg93His)
c.233G>A (p.Arg78His)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.48587292G>CCA406708766SULT2B1c.278G>C (p.Arg93Pro)
c.233G>C (p.Arg78Pro)
19g.48587292G=CA2339970793SULT2B1c.278G= (p.Arg93=)
c.233G= (p.Arg78=)
19g.48587292G>TCA309383607SULT2B1c.278G>T (p.Arg93Leu)
c.233G>T (p.Arg78Leu)
dbSNP gnomAD v4
19g.48587293C>ACA508042646SULT2B1c.279C>A (p.Arg93=)
c.234C>A (p.Arg78=)

Number of alleles fetched