Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.30233692C>ACA126289ARL14EP-DT,FSHBc.282C>A (p.Tyr94Ter)
n.463+83198G>T
n.284+83198G>T
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.30233692C=CA1961322278ARL14EP-DT,FSHBc.282C= (p.Tyr94=)
n.463+83198G=
n.284+83198G=
11g.30233692C>GCA380084350ARL14EP-DT,FSHBc.282C>G (p.Tyr94Ter)
n.463+83198G>C
n.284+83198G>C
11g.30233692C>TCA473783156ARL14EP-DT,FSHBc.282C>T (p.Tyr94=)
n.463+83198G>A
n.284+83198G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.30233693C>ACA380084351ARL14EP-DT,FSHBc.283C>A (p.Pro95Thr)
n.463+83197G>T
n.284+83197G>T
COSMIC
11g.30233693C=CA1961322279ARL14EP-DT,FSHBc.283C= (p.Pro95=)
n.463+83197G=
n.284+83197G=
11g.30233693C>GCA380084352ARL14EP-DT,FSHBc.283C>G (p.Pro95Ala)
n.463+83197G>C
n.284+83197G>C
11g.30233693C>TCA5930792ARL14EP-DT,FSHBc.283C>T (p.Pro95Ser)
n.463+83197G>A
n.284+83197G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.30233694C>ACA380084353ARL14EP-DT,FSHBc.284C>A (p.Pro95Gln)
n.463+83196G>T
n.284+83196G>T
11g.30233694C>GCA380084354ARL14EP-DT,FSHBc.284C>G (p.Pro95Arg)
n.463+83196G>C
n.284+83196G>C
11g.30233694C>TCA380084355ARL14EP-DT,FSHBc.284C>T (p.Pro95Leu)
n.463+83196G>A
n.284+83196G>A
11g.30233695A>CCA473783160ARL14EP-DT,FSHBc.285A>C (p.Pro95=)
n.463+83195T>G
n.284+83195T>G
11g.30233695A>GCA473783161ARL14EP-DT,FSHBc.285A>G (p.Pro95=)
n.463+83195T>C
n.284+83195T>C
gnomAD v4
11g.30233695A>TCA473783162ARL14EP-DT,FSHBc.285A>T (p.Pro95=)
n.463+83195T>A
n.284+83195T>A
COSMIC
11g.30233696G>ACA5930793ARL14EP-DT,FSHBc.286G>A (p.Val96Met)
n.463+83194C>T
n.284+83194C>T
dbSNP ExAC gnomAD v2 gnomAD v4
11g.30233696G>CCA380084356ARL14EP-DT,FSHBc.286G>C (p.Val96Leu)
n.463+83194C>G
n.284+83194C>G
11g.30233696G=CA1961322280ARL14EP-DT,FSHBc.286G= (p.Val96=)
n.463+83194C=
n.284+83194C=
11g.30233696G>TCA380084357ARL14EP-DT,FSHBc.286G>T (p.Val96Leu)
n.463+83194C>A
n.284+83194C>A
11g.30233697T>ACA380084360ARL14EP-DT,FSHBc.287T>A (p.Val96Glu)
n.463+83193A>T
n.284+83193A>T
11g.30233697T>CCA380084359ARL14EP-DT,FSHBc.287T>C (p.Val96Ala)
n.463+83193A>G
n.284+83193A>G
ClinVar
11g.30233697T>GCA380084358ARL14EP-DT,FSHBc.287T>G (p.Val96Gly)
n.463+83193A>C
n.284+83193A>C
gnomAD v4
11g.30233698G>ACA473783166ARL14EP-DT,FSHBc.288G>A (p.Val96=)
n.463+83192C>T
n.284+83192C>T
gnomAD v4
11g.30233698G>CCA473783164ARL14EP-DT,FSHBc.288G>C (p.Val96=)
n.463+83192C>G
n.284+83192C>G
11g.30233698G>TCA473783163ARL14EP-DT,FSHBc.288G>T (p.Val96=)
n.463+83192C>A
n.284+83192C>A
11g.30233699delCA2695213706ARL14EP-DT,FSHBc.289del (p.Ala97ProfsTer?)
n.463+83192del
n.284+83192del
11g.30233699G>ACA380084361ARL14EP-DT,FSHBc.289G>A (p.Ala97Thr)
n.463+83191C>T
n.284+83191C>T
11g.30233699G>CCA380084363ARL14EP-DT,FSHBc.289G>C (p.Ala97Pro)
n.463+83191C>G
n.284+83191C>G
11g.30233699G=CA1961322281ARL14EP-DT,FSHBc.289G= (p.Ala97=)
n.463+83191C=
n.284+83191C=
11g.30233699G>TCA380084362ARL14EP-DT,FSHBc.289G>T (p.Ala97Ser)
n.463+83191C>A
n.284+83191C>A
dbSNP gnomAD v3 gnomAD v4
11g.30233700C>ACA380084364ARL14EP-DT,FSHBc.290C>A (p.Ala97Asp)
n.463+83190G>T
n.284+83190G>T
gnomAD v4 COSMIC
11g.30233700C>GCA380084365ARL14EP-DT,FSHBc.290C>G (p.Ala97Gly)
n.463+83190G>C
n.284+83190G>C
11g.30233700C>TCA380084366ARL14EP-DT,FSHBc.290C>T (p.Ala97Val)
n.463+83190G>A
n.284+83190G>A
gnomAD v4
11g.30233701C>ACA220135128ARL14EP-DT,FSHBc.291C>A (p.Ala97=)
n.463+83189G>T
n.284+83189G>T
dbSNP
11g.30233701C=CA1961322282ARL14EP-DT,FSHBc.291C= (p.Ala97=)
n.463+83189G=
n.284+83189G=
11g.30233701C>GCA473783170ARL14EP-DT,FSHBc.291C>G (p.Ala97=)
n.463+83189G>C
n.284+83189G>C
11g.30233701C>TCA473783171ARL14EP-DT,FSHBc.291C>T (p.Ala97=)
n.463+83189G>A
n.284+83189G>A
COSMIC
11g.30233702A>CCA380084367ARL14EP-DT,FSHBc.292A>C (p.Thr98Pro)
n.463+83188T>G
n.284+83188T>G
11g.30233702A>GCA380084368ARL14EP-DT,FSHBc.292A>G (p.Thr98Ala)
n.463+83188T>C
n.284+83188T>C
11g.30233702A>TCA380084369ARL14EP-DT,FSHBc.292A>T (p.Thr98Ser)
n.463+83188T>A
n.284+83188T>A
11g.30233703C>ACA380084370ARL14EP-DT,FSHBc.293C>A (p.Thr98Asn)
n.463+83187G>T
n.284+83187G>T
11g.30233703C=CA1961322283ARL14EP-DT,FSHBc.293C= (p.Thr98=)
n.463+83187G=
n.284+83187G=
11g.30233703C>GCA380084371ARL14EP-DT,FSHBc.293C>G (p.Thr98Ser)
n.463+83187G>C
n.284+83187G>C
11g.30233703C>TCA5930794ARL14EP-DT,FSHBc.293C>T (p.Thr98Ile)
n.463+83187G>A
n.284+83187G>A
dbSNP ExAC gnomAD v3 gnomAD v4
11g.30233704C>ACA473783173ARL14EP-DT,FSHBc.294C>A (p.Thr98=)
n.463+83186G>T
n.284+83186G>T
11g.30233704C=CA1961322284ARL14EP-DT,FSHBc.294C= (p.Thr98=)
n.463+83186G=
n.284+83186G=
11g.30233704C>GCA473783174ARL14EP-DT,FSHBc.294C>G (p.Thr98=)
n.463+83186G>C
n.284+83186G>C
11g.30233704C>TCA5930795ARL14EP-DT,FSHBc.294C>T (p.Thr98=)
n.463+83186G>A
n.284+83186G>A
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
11g.30233705C>ACA380084372ARL14EP-DT,FSHBc.295C>A (p.Gln99Lys)
n.463+83185G>T
n.284+83185G>T
11g.30233705C=CA1961322285ARL14EP-DT,FSHBc.295C= (p.Gln99=)
n.463+83185G=
n.284+83185G=
11g.30233705C>GCA380084373ARL14EP-DT,FSHBc.295C>G (p.Gln99Glu)
n.463+83185G>C
n.284+83185G>C

Number of alleles fetched