Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.59654249_59654254delCA2574558623SLC16A9c.775_780del (p.Val259_Thr260del)
c.514_519del (p.Val172_Thr173del)
10g.59654253G>ACA377064381SLC16A9c.773C>T (p.Thr258Ile)
c.512C>T (p.Thr171Ile)
10g.59654253G>CCA377064382SLC16A9c.773C>G (p.Thr258Arg)
c.512C>G (p.Thr171Arg)
10g.59654253G=CA1913561201SLC16A9c.773C= (p.Thr258=)
c.512C= (p.Thr171=)
10g.59654253G>TCA5509949SLC16A9c.773C>A (p.Thr258Lys)
c.512C>A (p.Thr171Lys)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.59654254T>ACA377064383SLC16A9c.772A>T (p.Thr258Ser)
c.511A>T (p.Thr171Ser)
dbSNP
10g.59654254T>CCA377064384SLC16A9c.772A>G (p.Thr258Ala)
c.511A>G (p.Thr171Ala)
10g.59654254T>GCA377064385SLC16A9c.772A>C (p.Thr258Pro)
c.511A>C (p.Thr171Pro)
10g.59654255G>ACA470000960SLC16A9c.771C>T (p.Pro257=)
c.510C>T (p.Pro170=)
10g.59654255G>CCA470000962SLC16A9c.771C>G (p.Pro257=)
c.510C>G (p.Pro170=)
10g.59654255G>TCA470000963SLC16A9c.771C>A (p.Pro257=)
c.510C>A (p.Pro170=)
10g.59654256G>ACA377064386SLC16A9c.770C>T (p.Pro257Leu)
c.509C>T (p.Pro170Leu)
gnomAD v4
10g.59654256G>CCA377064387SLC16A9c.770C>G (p.Pro257Arg)
c.509C>G (p.Pro170Arg)
gnomAD v4
10g.59654256G>TCA377064388SLC16A9c.770C>A (p.Pro257His)
c.509C>A (p.Pro170His)
10g.59654257G>ACA377064390SLC16A9c.769C>T (p.Pro257Ser)
c.508C>T (p.Pro170Ser)
10g.59654257G>CCA377064391SLC16A9c.769C>G (p.Pro257Ala)
c.508C>G (p.Pro170Ala)
10g.59654257G>TCA377064389SLC16A9c.769C>A (p.Pro257Thr)
c.508C>A (p.Pro170Thr)
10g.59654258G>ACA470000964SLC16A9c.768C>T (p.Asn256=)
c.507C>T (p.Asn169=)
10g.59654258G>CCA377064392SLC16A9c.768C>G (p.Asn256Lys)
c.507C>G (p.Asn169Lys)
10g.59654258G>TCA377064393SLC16A9c.768C>A (p.Asn256Lys)
c.507C>A (p.Asn169Lys)
10g.59654259T>ACA5509950SLC16A9c.767A>T (p.Asn256Ile)
c.506A>T (p.Asn169Ile)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.59654259T>CCA377064394SLC16A9c.767A>G (p.Asn256Ser)
c.506A>G (p.Asn169Ser)
10g.59654259T>GCA377064395SLC16A9c.767A>C (p.Asn256Thr)
c.506A>C (p.Asn169Thr)
10g.59654259T=CA1913561206SLC16A9c.767A= (p.Asn256=)
c.506A= (p.Asn169=)
10g.59654260T>ACA377064398SLC16A9c.766A>T (p.Asn256Tyr)
c.505A>T (p.Asn169Tyr)
10g.59654260T>CCA377064396SLC16A9c.766A>G (p.Asn256Asp)
c.505A>G (p.Asn169Asp)
10g.59654260T>GCA377064397SLC16A9c.766A>C (p.Asn256His)
c.505A>C (p.Asn169His)
10g.59654261T>ACA377064399SLC16A9c.765A>T (p.Lys255Asn)
c.504A>T (p.Lys168Asn)
10g.59654261T>CCA470000966SLC16A9c.765A>G (p.Lys255=)
c.504A>G (p.Lys168=)
gnomAD v4
10g.59654261T>GCA377064400SLC16A9c.765A>C (p.Lys255Asn)
c.504A>C (p.Lys168Asn)
10g.59654262T>ACA377064401SLC16A9c.764A>T (p.Lys255Ile)
c.503A>T (p.Lys168Ile)
10g.59654262T>CCA377064402SLC16A9c.764A>G (p.Lys255Arg)
c.503A>G (p.Lys168Arg)
10g.59654262T>GCA377064403SLC16A9c.764A>C (p.Lys255Thr)
c.503A>C (p.Lys168Thr)
gnomAD v4
10g.59654263T>ACA377064406SLC16A9c.763A>T (p.Lys255Ter)
c.502A>T (p.Lys168Ter)
10g.59654263T>CCA377064405SLC16A9c.763A>G (p.Lys255Glu)
c.502A>G (p.Lys168Glu)
10g.59654263T>GCA377064404SLC16A9c.763A>C (p.Lys255Gln)
c.502A>C (p.Lys168Gln)
10g.59654264A>CCA377064407SLC16A9c.762T>G (p.His254Gln)
c.501T>G (p.His167Gln)
10g.59654264A>GCA470000969SLC16A9c.762T>C (p.His254=)
c.501T>C (p.His167=)
gnomAD v4
10g.59654264A>TCA377064408SLC16A9c.762T>A (p.His254Gln)
c.501T>A (p.His167Gln)
10g.59654265T>ACA377064409SLC16A9c.761A>T (p.His254Leu)
c.500A>T (p.His167Leu)
10g.59654265T>CCA377064410SLC16A9c.761A>G (p.His254Arg)
c.500A>G (p.His167Arg)
10g.59654265T>GCA377064411SLC16A9c.761A>C (p.His254Pro)
c.500A>C (p.His167Pro)
10g.59654266G>ACA377064412SLC16A9c.760C>T (p.His254Tyr)
c.499C>T (p.His167Tyr)
COSMIC
10g.59654266G>CCA377064413SLC16A9c.760C>G (p.His254Asp)
c.499C>G (p.His167Asp)
10g.59654266G>TCA377064414SLC16A9c.760C>A (p.His254Asn)
c.499C>A (p.His167Asn)
10g.59654267A>CCA470000974SLC16A9c.759T>G (p.Leu253=)
c.498T>G (p.Leu166=)
10g.59654267A>GCA470000975SLC16A9c.759T>C (p.Leu253=)
c.498T>C (p.Leu166=)
10g.59654267A>TCA470000976SLC16A9c.759T>A (p.Leu253=)
c.498T>A (p.Leu166=)
10g.59654268A=CA1913561211SLC16A9c.758T= (p.Leu253=)
c.497T= (p.Leu166=)
10g.59654268A>CCA377064415SLC16A9c.758T>G (p.Leu253Arg)
c.497T>G (p.Leu166Arg)

Number of alleles fetched