Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.47862453A>CCA371162357PRKDCc.5839T>G (p.Cys1947Gly)
n.505T>G
8g.47862453A>GCA371162359PRKDCc.5839T>C (p.Cys1947Arg)
n.505T>C
8g.47862453A>TCA371162355PRKDCc.5839T>A (p.Cys1947Ser)
n.505T>A
8g.47862454G>ACA460607561PRKDCc.5838C>T (p.Asn1946=)
n.504C>T
8g.47862454G>CCA371162360PRKDCc.5838C>G (p.Asn1946Lys)
n.504C>G
8g.47862454G>TCA371162362PRKDCc.5838C>A (p.Asn1946Lys)
n.504C>A
8g.47862455T>ACA371162364PRKDCc.5837A>T (p.Asn1946Ile)
n.503A>T
8g.47862455T>CCA4740559PRKDCc.5837A>G (p.Asn1946Ser)
n.503A>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.47862455T>GCA371162365PRKDCc.5837A>C (p.Asn1946Thr)
n.503A>C
gnomAD v4
8g.47862455T=CA1781860488PRKDCc.5837A= (p.Asn1946=)
n.503A=
8g.47862456T>ACA371162367PRKDCc.5836A>T (p.Asn1946Tyr)
n.502A>T
8g.47862456T>CCA371162368PRKDCc.5836A>G (p.Asn1946Asp)
n.502A>G
ClinVar
8g.47862456T>GCA371162370PRKDCc.5836A>C (p.Asn1946His)
n.502A>C
ClinVar
8g.47862457G>ACA460607562PRKDCc.5835C>T (p.Tyr1945=)
n.501C>T
8g.47862457G>CCA371162372PRKDCc.5835C>G (p.Tyr1945Ter)
n.501C>G
8g.47862457G>TCA371162374PRKDCc.5835C>A (p.Tyr1945Ter)
n.501C>A
8g.47862458T>ACA371162375PRKDCc.5834A>T (p.Tyr1945Phe)
n.500A>T
8g.47862458T>CCA371162376PRKDCc.5834A>G (p.Tyr1945Cys)
n.500A>G
8g.47862458T>GCA371162378PRKDCc.5834A>C (p.Tyr1945Ser)
n.500A>C
8g.47862459A>CCA371162383PRKDCc.5833T>G (p.Tyr1945Asp)
n.499T>G
8g.47862459A>GCA371162382PRKDCc.5833T>C (p.Tyr1945His)
n.499T>C
gnomAD v4
8g.47862459A>TCA371162380PRKDCc.5833T>A (p.Tyr1945Asn)
n.499T>A
8g.47862460T>ACA460607563PRKDCc.5832A>T (p.Ala1944=)
n.498A>T
8g.47862460T>CCA460607565PRKDCc.5832A>G (p.Ala1944=)
n.498A>G
COSMIC
8g.47862460T>GCA460607564PRKDCc.5832A>C (p.Ala1944=)
n.498A>C
8g.47862461G>ACA371162385PRKDCc.5831C>T (p.Ala1944Val)
n.497C>T
8g.47862461G>CCA371162386PRKDCc.5831C>G (p.Ala1944Gly)
n.497C>G
8g.47862461G>TCA371162388PRKDCc.5831C>A (p.Ala1944Glu)
n.497C>A
8g.47862462C>ACA371162390PRKDCc.5830G>T (p.Ala1944Ser)
n.496G>T
8g.47862462C>GCA371162391PRKDCc.5830G>C (p.Ala1944Pro)
n.496G>C
8g.47862462C>TCA371162393PRKDCc.5830G>A (p.Ala1944Thr)
n.496G>A
8g.47862463T>ACA460607566PRKDCc.5829A>T (p.Ala1943=)
n.495A>T
dbSNP gnomAD v3 gnomAD v4
8g.47862463T>CCA460607567PRKDCc.5829A>G (p.Ala1943=)
n.495A>G
ClinVar dbSNP
8g.47862463T>GCA460607568PRKDCc.5829A>C (p.Ala1943=)
n.495A>C
8g.47862463T=CA1781860498PRKDCc.5829A= (p.Ala1943=)
n.495A=
8g.47862464G>ACA371162395PRKDCc.5828C>T (p.Ala1943Val)
n.494C>T
gnomAD v4
8g.47862464G>CCA371162396PRKDCc.5828C>G (p.Ala1943Gly)
n.494C>G
8g.47862464G>TCA371162397PRKDCc.5828C>A (p.Ala1943Glu)
n.494C>A
8g.47862465C>ACA4740560PRKDCc.5827G>T (p.Ala1943Ser)
n.493G>T
dbSNP ExAC gnomAD v2 gnomAD v4
8g.47862465C=CA1781860504PRKDCc.5827G= (p.Ala1943=)
n.493G=
8g.47862465C>GCA371162400PRKDCc.5827G>C (p.Ala1943Pro)
n.493G>C
8g.47862465C>TCA371162401PRKDCc.5827G>A (p.Ala1943Thr)
n.493G>A
8g.47862466A>CCA371162403PRKDCc.5826T>G (p.Cys1942Trp)
n.492T>G
8g.47862466A>GCA460607569PRKDCc.5826T>C (p.Cys1942=)
n.492T>C
8g.47862466A>TCA371162404PRKDCc.5826T>A (p.Cys1942Ter)
n.492T>A
8g.47862467C>ACA371162407PRKDCc.5825G>T (p.Cys1942Phe)
n.491G>T
8g.47862467C>GCA371162409PRKDCc.5825G>C (p.Cys1942Ser)
n.491G>C
8g.47862467C>TCA371162406PRKDCc.5825G>A (p.Cys1942Tyr)
n.491G>A
8g.47862468A>CCA371162410PRKDCc.5824T>G (p.Cys1942Gly)
n.490T>G
8g.47862468A>GCA371162411PRKDCc.5824T>C (p.Cys1942Arg)
n.490T>C

Number of alleles fetched