Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.51765768T>ACA384887436SCN8Ac.2642T>A (p.Val881Glu)
c.489T>A
c.646T>A
n.2770T>A
c.2675T>A (p.Val892Glu)
12g.51765768T>CCA318258SCN8Ac.2642T>C (p.Val881Ala)
c.489T>C
c.646T>C
n.2770T>C
c.2675T>C (p.Val892Ala)
dbSNP
12g.51765768T>GCA384887439SCN8Ac.2642T>G (p.Val881Gly)
c.489T>G
c.646T>G
n.2770T>G
c.2675T>G (p.Val892Gly)
12g.51765768T=CA2036184091SCN8Ac.2642T= (p.Val881=)
c.489T=
c.646T=
n.2770T=
c.2675T= (p.Val892=)
12g.51765769G>ACA480061307SCN8Ac.2643G>A (p.Val881=)
c.490G>A
c.647G>A
n.2771G>A
c.2676G>A (p.Val892=)
dbSNP gnomAD v2 gnomAD v4
12g.51765769G>CCA480061309SCN8Ac.2643G>C (p.Val881=)
c.490G>C
c.647G>C
n.2771G>C
c.2676G>C (p.Val892=)
12g.51765769G=CA2036184092SCN8Ac.2643G= (p.Val881=)
c.490G=
c.647G=
n.2771G=
c.2676G= (p.Val892=)
12g.51765769G>TCA480061310SCN8Ac.2643G>T (p.Val881=)
c.490G>T
c.647G>T
n.2771G>T
c.2676G>T (p.Val892=)
12g.51765770C>ACA384887443SCN8Ac.2644C>A (p.Leu882Met)
c.491C>A
c.648C>A
n.2772C>A
c.2677C>A (p.Leu893Met)
12g.51765770C>GCA384887446SCN8Ac.2644C>G (p.Leu882Val)
c.491C>G
c.648C>G
n.2772C>G
c.2677C>G (p.Leu893Val)
12g.51765770C>TCA480061312SCN8Ac.2644C>T (p.Leu882=)
c.491C>T
c.648C>T
n.2772C>T
c.2677C>T (p.Leu893=)
12g.51765771T>ACA384887451SCN8Ac.2645T>A (p.Leu882Gln)
c.492T>A
c.649T>A
n.2773T>A
c.2678T>A (p.Leu893Gln)
12g.51765771T>CCA384887461SCN8Ac.2645T>C (p.Leu882Pro)
c.492T>C
c.649T>C
n.2773T>C
c.2678T>C (p.Leu893Pro)
12g.51765771T>GCA384887464SCN8Ac.2645T>G (p.Leu882Arg)
c.492T>G
c.649T>G
n.2773T>G
c.2678T>G (p.Leu893Arg)
12g.51765772G>ACA480061314SCN8Ac.2646G>A (p.Leu882=)
c.493G>A
c.650G>A
n.2774G>A
c.2679G>A (p.Leu893=)
12g.51765772G>CCA480061315SCN8Ac.2646G>C (p.Leu882=)
c.493G>C
c.650G>C
n.2774G>C
c.2679G>C (p.Leu893=)
12g.51765772G>TCA480061317SCN8Ac.2646G>T (p.Leu882=)
c.493G>T
c.650G>T
n.2774G>T
c.2679G>T (p.Leu893=)
COSMIC COSMIC
12g.51765773G>ACA384887477SCN8Ac.2647G>A (p.Ala883Thr)
c.494G>A
c.651G>A
n.2775G>A
c.2680G>A (p.Ala894Thr)
12g.51765773G>CCA384887481SCN8Ac.2647G>C (p.Ala883Pro)
c.494G>C
c.651G>C
n.2775G>C
c.2680G>C (p.Ala894Pro)
12g.51765773G>TCA384887470SCN8Ac.2647G>T (p.Ala883Ser)
c.494G>T
c.651G>T
n.2775G>T
c.2680G>T (p.Ala894Ser)
12g.51765774C>ACA384887482SCN8Ac.2648C>A (p.Ala883Asp)
c.495C>A
c.652C>A
n.2776C>A
c.2681C>A (p.Ala894Asp)
12g.51765774C>GCA384887484SCN8Ac.2648C>G (p.Ala883Gly)
c.495C>G
c.652C>G
n.2776C>G
c.2681C>G (p.Ala894Gly)
12g.51765774C>TCA384887483SCN8Ac.2648C>T (p.Ala883Val)
c.495C>T
c.652C>T
n.2776C>T
c.2681C>T (p.Ala894Val)
12g.51765775C>ACA480061318SCN8Ac.2649C>A (p.Ala883=)
c.496C>A
c.653C>A
n.2777C>A
c.2682C>A (p.Ala894=)
12g.51765775C>GCA480061320SCN8Ac.2649C>G (p.Ala883=)
c.496C>G
c.653C>G
n.2777C>G
c.2682C>G (p.Ala894=)
12g.51765775C>TCA480061322SCN8Ac.2649C>T (p.Ala883=)
c.496C>T
c.653C>T
n.2777C>T
c.2682C>T (p.Ala894=)
12g.51765776A>CCA384887487SCN8Ac.2650A>C (p.Ile884Leu)
c.497A>C
c.654A>C
n.2778A>C
c.2683A>C (p.Ile895Leu)
12g.51765776A>GCA384887488SCN8Ac.2650A>G (p.Ile884Val)
c.497A>G
c.654A>G
n.2778A>G
c.2683A>G (p.Ile895Val)
12g.51765776A>TCA384887489SCN8Ac.2650A>T (p.Ile884Phe)
c.497A>T
c.654A>T
n.2778A>T
c.2683A>T (p.Ile895Phe)
12g.51765777T>ACA384887490SCN8Ac.2651T>A (p.Ile884Asn)
c.498T>A
c.655T>A
n.2779T>A
c.2684T>A (p.Ile895Asn)
12g.51765777T>CCA384887491SCN8Ac.2651T>C (p.Ile884Thr)
c.498T>C
c.655T>C
n.2779T>C
c.2684T>C (p.Ile895Thr)
12g.51765777T>GCA384887494SCN8Ac.2651T>G (p.Ile884Ser)
c.498T>G
c.655T>G
n.2779T>G
c.2684T>G (p.Ile895Ser)
12g.51765778T>ACA480061327SCN8Ac.2652T>A (p.Ile884=)
c.499T>A
c.656T>A
n.2780T>A
c.2685T>A (p.Ile895=)
12g.51765778T>CCA480061329SCN8Ac.2652T>C (p.Ile884=)
c.499T>C
c.656T>C
n.2780T>C
c.2685T>C (p.Ile895=)
12g.51765778T>GCA384887498SCN8Ac.2652T>G (p.Ile884Met)
c.499T>G
c.656T>G
n.2780T>G
c.2685T>G (p.Ile895Met)
12g.51765779A>CCA384887500SCN8Ac.2653A>C (p.Ile885Leu)
c.500A>C
c.657A>C
n.2781A>C
c.2686A>C (p.Ile896Leu)
12g.51765779A>GCA384887502SCN8Ac.2653A>G (p.Ile885Val)
c.500A>G
c.657A>G
n.2781A>G
c.2686A>G (p.Ile896Val)
gnomAD v4
12g.51765779A>TCA384887505SCN8Ac.2653A>T (p.Ile885Phe)
c.500A>T
c.657A>T
n.2781A>T
c.2686A>T (p.Ile896Phe)
12g.51765780T>ACA384887507SCN8Ac.2654T>A (p.Ile885Asn)
c.501T>A
c.658T>A
n.2782T>A
c.2687T>A (p.Ile896Asn)
12g.51765780T>CCA384887511SCN8Ac.2654T>C (p.Ile885Thr)
c.501T>C
c.658T>C
n.2782T>C
c.2687T>C (p.Ile896Thr)
ClinVar dbSNP
12g.51765780T>GCA384887514SCN8Ac.2654T>G (p.Ile885Ser)
c.501T>G
c.658T>G
n.2782T>G
c.2687T>G (p.Ile896Ser)
12g.51765780T=CA2036184098SCN8Ac.2654T= (p.Ile885=)
c.501T=
c.658T=
n.2782T=
c.2687T= (p.Ile896=)
12g.51765781T>ACA480061331SCN8Ac.2655T>A (p.Ile885=)
c.502T>A
c.659T>A
n.2783T>A
c.2688T>A (p.Ile896=)
12g.51765781T>CCA480061332SCN8Ac.2655T>C (p.Ile885=)
c.502T>C
c.659T>C
n.2783T>C
c.2688T>C (p.Ile896=)
12g.51765781T>GCA384887517SCN8Ac.2655T>G (p.Ile885Met)
c.502T>G
c.659T>G
n.2783T>G
c.2688T>G (p.Ile896Met)
12g.51765782G>ACA384887521SCN8Ac.2656G>A (p.Val886Ile)
c.503G>A
c.660G>A
n.2784G>A
c.2689G>A (p.Val897Ile)
12g.51765782G>CCA384887525SCN8Ac.2656G>C (p.Val886Leu)
c.503G>C
c.660G>C
n.2784G>C
c.2689G>C (p.Val897Leu)
12g.51765782G>TCA384887527SCN8Ac.2656G>T (p.Val886Phe)
c.503G>T
c.660G>T
n.2784G>T
c.2689G>T (p.Val897Phe)
12g.51765783T>ACA384887528SCN8Ac.2657T>A (p.Val886Asp)
c.504T>A
c.661T>A
n.2785T>A
c.2690T>A (p.Val897Asp)
12g.51765783T>CCA384887529SCN8Ac.2657T>C (p.Val886Ala)
c.504T>C
c.661T>C
n.2785T>C
c.2690T>C (p.Val897Ala)

Number of alleles fetched