Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.47929865T>ACA460607329PRKDCc.2040A>T (p.Ile680=)
8g.47929865T>CCA4741573PRKDCc.2040A>G (p.Ile680Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.47929865T>GCA460607328PRKDCc.2040A>C (p.Ile680=)
8g.47929865T=CA1781903315PRKDCc.2040A= (p.Ile680=)
8g.47929866A>CCA371164097PRKDCc.2039T>G (p.Ile680Arg)
8g.47929866A>GCA371164098PRKDCc.2039T>C (p.Ile680Thr)
8g.47929866A>TCA371164099PRKDCc.2039T>A (p.Ile680Lys)
8g.47929867T>ACA371164101PRKDCc.2038A>T (p.Ile680Leu)
8g.47929867T>CCA371164102PRKDCc.2038A>G (p.Ile680Val)
8g.47929867T>GCA371164100PRKDCc.2038A>C (p.Ile680Leu)
8g.47929868T>ACA371164103PRKDCc.2037A>T (p.Lys679Asn)
8g.47929868T>CCA460607331PRKDCc.2037A>G (p.Lys679=)
ClinVar
8g.47929868T>GCA371164104PRKDCc.2037A>C (p.Lys679Asn)
gnomAD v4
8g.47929869T>ACA371164105PRKDCc.2036A>T (p.Lys679Ile)
8g.47929869T>CCA371164106PRKDCc.2036A>G (p.Lys679Arg)
8g.47929869T>GCA371164107PRKDCc.2036A>C (p.Lys679Thr)
8g.47929870T>ACA371164110PRKDCc.2035A>T (p.Lys679Ter)
8g.47929870T>CCA371164108PRKDCc.2035A>G (p.Lys679Glu)
ClinVar dbSNP gnomAD v2 gnomAD v4
8g.47929870T>GCA371164109PRKDCc.2035A>C (p.Lys679Gln)
8g.47929870T=CA1781903316PRKDCc.2035A= (p.Lys679=)
8g.47929871C>ACA371164111PRKDCc.2034G>T (p.Lys678Asn)
8g.47929871C>GCA371164112PRKDCc.2034G>C (p.Lys678Asn)
8g.47929871C>TCA460607333PRKDCc.2034G>A (p.Lys678=)
COSMIC
8g.47929872T>ACA371164113PRKDCc.2033A>T (p.Lys678Met)
8g.47929872T>CCA371164114PRKDCc.2033A>G (p.Lys678Arg)
8g.47929872T>GCA371164115PRKDCc.2033A>C (p.Lys678Thr)
8g.47929873T>ACA371164118PRKDCc.2032A>T (p.Lys678Ter)
8g.47929873T>CCA371164117PRKDCc.2032A>G (p.Lys678Glu)
dbSNP gnomAD v3 gnomAD v4
8g.47929873T>GCA371164116PRKDCc.2032A>C (p.Lys678Gln)
8g.47929873T=CA1781903317PRKDCc.2032A= (p.Lys678=)
8g.47929874G>ACA460607336PRKDCc.2031C>T (p.Ala677=)
dbSNP gnomAD v4
8g.47929874G>CCA460607337PRKDCc.2031C>G (p.Ala677=)
8g.47929874G=CA1781903318PRKDCc.2031C= (p.Ala677=)
8g.47929874G>TCA460607338PRKDCc.2031C>A (p.Ala677=)
gnomAD v4
8g.47929875G>ACA371164119PRKDCc.2030C>T (p.Ala677Val)
ClinVar
8g.47929875G>CCA371164120PRKDCc.2030C>G (p.Ala677Gly)
8g.47929875G>TCA371164121PRKDCc.2030C>A (p.Ala677Asp)
8g.47929876C>ACA371164122PRKDCc.2029G>T (p.Ala677Ser)
gnomAD v4
8g.47929876C=CA1781903319PRKDCc.2029G= (p.Ala677=)
8g.47929876C>GCA371164123PRKDCc.2029G>C (p.Ala677Pro)
8g.47929876C>TCA176164563PRKDCc.2029G>A (p.Ala677Thr)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.47929877A=CA1781903320PRKDCc.2028T= (p.Asn676=)
8g.47929877A>CCA371164124PRKDCc.2028T>G (p.Asn676Lys)
8g.47929877A>GCA460607342PRKDCc.2028T>C (p.Asn676=)
ClinVar dbSNP gnomAD v4
8g.47929877A>TCA4741574PRKDCc.2028T>A (p.Asn676Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
8g.47929878T>ACA371164125PRKDCc.2027A>T (p.Asn676Ile)
8g.47929878T>CCA176164567PRKDCc.2027A>G (p.Asn676Ser)
ClinVar dbSNP
8g.47929878T>GCA371164126PRKDCc.2027A>C (p.Asn676Thr)
8g.47929878T=CA1781903321PRKDCc.2027A= (p.Asn676=)
8g.47929879T>ACA371164128PRKDCc.2026A>T (p.Asn676Tyr)

Number of alleles fetched