Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.47789037C>ACA371132281PRKDCn.1344G>T
c.3448G>T (p.Asp1150Tyr)
c.10771G>T (p.Asp3591Tyr)
c.10774G>T (p.Asp3592Tyr)
8g.47789037C>GCA371132282PRKDCn.1344G>C
c.3448G>C (p.Asp1150His)
c.10771G>C (p.Asp3591His)
c.10774G>C (p.Asp3592His)
8g.47789037C>TCA371132283PRKDCn.1344G>A
c.3448G>A (p.Asp1150Asn)
c.10771G>A (p.Asp3591Asn)
c.10774G>A (p.Asp3592Asn)
 gnomAD v4
8g.47789038A>CCA371132284PRKDCn.1343T>G
c.3447T>G (p.Asn1149Lys)
c.10770T>G (p.Asn3590Lys)
c.10773T>G (p.Asn3591Lys)
 gnomAD v4
8g.47789038A>GCA460603931PRKDCn.1343T>C
c.3447T>C (p.Asn1149=)
c.10770T>C (p.Asn3590=)
c.10773T>C (p.Asn3591=)
8g.47789038A>TCA371132285PRKDCn.1343T>A
c.3447T>A (p.Asn1149Lys)
c.10770T>A (p.Asn3590Lys)
c.10773T>A (p.Asn3591Lys)
8g.47789039T>ACA371132286PRKDCn.1342A>T
c.3446A>T (p.Asn1149Ile)
c.10769A>T (p.Asn3590Ile)
c.10772A>T (p.Asn3591Ile)
8g.47789039T>CCA371132287PRKDCn.1342A>G
c.3446A>G (p.Asn1149Ser)
c.10769A>G (p.Asn3590Ser)
c.10772A>G (p.Asn3591Ser)
 dbSNP
8g.47789039T>GCA371132288PRKDCn.1342A>C
c.3446A>C (p.Asn1149Thr)
c.10769A>C (p.Asn3590Thr)
c.10772A>C (p.Asn3591Thr)
8g.47789039T=CA1781813537PRKDCn.1342A=
c.3446A= (p.Asn1149=)
c.10769A= (p.Asn3590=)
c.10772A= (p.Asn3591=)
8g.47789040T>ACA371132289PRKDCn.1341A>T
c.3445A>T (p.Asn1149Tyr)
c.10768A>T (p.Asn3590Tyr)
c.10771A>T (p.Asn3591Tyr)
8g.47789040T>CCA371132291PRKDCn.1341A>G
c.3445A>G (p.Asn1149Asp)
c.10768A>G (p.Asn3590Asp)
c.10771A>G (p.Asn3591Asp)
 ClinVar
8g.47789040T>GCA371132290PRKDCn.1341A>C
c.3445A>C (p.Asn1149His)
c.10768A>C (p.Asn3590His)
c.10771A>C (p.Asn3591His)
8g.47789041G>ACA460603934PRKDCn.1340C>T
c.3444C>T (p.Ser1148=)
c.10767C>T (p.Ser3589=)
c.10770C>T (p.Ser3590=)
 gnomAD v4
8g.47789041G>CCA371132292PRKDCn.1340C>G
c.3444C>G (p.Ser1148Arg)
c.10767C>G (p.Ser3589Arg)
c.10770C>G (p.Ser3590Arg)
8g.47789041G>TCA371132293PRKDCn.1340C>A
c.3444C>A (p.Ser1148Arg)
c.10767C>A (p.Ser3589Arg)
c.10770C>A (p.Ser3590Arg)
8g.47789042C>ACA371132294PRKDCn.1339G>T
c.3443G>T (p.Ser1148Ile)
c.10766G>T (p.Ser3589Ile)
c.10769G>T (p.Ser3590Ile)
8g.47789042C>GCA371132295PRKDCn.1339G>C
c.3443G>C (p.Ser1148Thr)
c.10766G>C (p.Ser3589Thr)
c.10769G>C (p.Ser3590Thr)
8g.47789042C>TCA371132296PRKDCn.1339G>A
c.3443G>A (p.Ser1148Asn)
c.10766G>A (p.Ser3589Asn)
c.10769G>A (p.Ser3590Asn)
 gnomAD v4
8g.47789043T>ACA371132297PRKDCn.1338A>T
c.3442A>T (p.Ser1148Cys)
c.10765A>T (p.Ser3589Cys)
c.10768A>T (p.Ser3590Cys)
 dbSNP
8g.47789043T>CCA371132298PRKDCn.1338A>G
c.3442A>G (p.Ser1148Gly)
c.10765A>G (p.Ser3589Gly)
c.10768A>G (p.Ser3590Gly)
8g.47789043T>GCA371132299PRKDCn.1338A>C
c.3442A>C (p.Ser1148Arg)
c.10765A>C (p.Ser3589Arg)
c.10768A>C (p.Ser3590Arg)
8g.47789043T=CA1781813538PRKDCn.1338A=
c.3442A= (p.Ser1148=)
c.10765A= (p.Ser3589=)
c.10768A= (p.Ser3590=)
8g.47789044C>ACA371132300PRKDCn.1337G>T
c.3441G>T (p.Trp1147Cys)
c.10764G>T (p.Trp3588Cys)
c.10767G>T (p.Trp3589Cys)
 dbSNP
8g.47789044C=CA1781813539PRKDCn.1337G=
c.3441G= (p.Trp1147=)
c.10764G= (p.Trp3588=)
c.10767G= (p.Trp3589=)
8g.47789044C>GCA371132301PRKDCn.1337G>C
c.3441G>C (p.Trp1147Cys)
c.10764G>C (p.Trp3588Cys)
c.10767G>C (p.Trp3589Cys)
8g.47789044C>TCA371132302PRKDCn.1337G>A
c.3441G>A (p.Trp1147Ter)
c.10764G>A (p.Trp3588Ter)
c.10767G>A (p.Trp3589Ter)
8g.47789045C>ACA371132305PRKDCn.1336G>T
c.3440G>T (p.Trp1147Leu)
c.10763G>T (p.Trp3588Leu)
c.10766G>T (p.Trp3589Leu)
8g.47789045C>GCA371132303PRKDCn.1336G>C
c.3440G>C (p.Trp1147Ser)
c.10763G>C (p.Trp3588Ser)
c.10766G>C (p.Trp3589Ser)
8g.47789045C>TCA371132304PRKDCn.1336G>A
c.3440G>A (p.Trp1147Ter)
c.10763G>A (p.Trp3588Ter)
c.10766G>A (p.Trp3589Ter)
8g.47789046A>CCA371132306PRKDCn.1335T>G
c.3439T>G (p.Trp1147Gly)
c.10762T>G (p.Trp3588Gly)
c.10765T>G (p.Trp3589Gly)
8g.47789046A>GCA371132307PRKDCn.1335T>C
c.3439T>C (p.Trp1147Arg)
c.10762T>C (p.Trp3588Arg)
c.10765T>C (p.Trp3589Arg)
8g.47789046A>TCA371132308PRKDCn.1335T>A
c.3439T>A (p.Trp1147Arg)
c.10762T>A (p.Trp3588Arg)
c.10765T>A (p.Trp3589Arg)
8g.47789047A>CCA371132309PRKDCn.1334T>G
c.3438T>G (p.Asp1146Glu)
c.10761T>G (p.Asp3587Glu)
c.10764T>G (p.Asp3588Glu)
8g.47789047A>GCA460603943PRKDCn.1334T>C
c.3438T>C (p.Asp1146=)
c.10761T>C (p.Asp3587=)
c.10764T>C (p.Asp3588=)
 gnomAD v4
8g.47789047A>TCA371132310PRKDCn.1334T>A
c.3438T>A (p.Asp1146Glu)
c.10761T>A (p.Asp3587Glu)
c.10764T>A (p.Asp3588Glu)
8g.47789048T>ACA371132311PRKDCn.1333A>T
c.3437A>T (p.Asp1146Val)
c.10760A>T (p.Asp3587Val)
c.10763A>T (p.Asp3588Val)
 gnomAD v4
8g.47789048T>CCA371132312PRKDCn.1333A>G
c.3437A>G (p.Asp1146Gly)
c.10760A>G (p.Asp3587Gly)
c.10763A>G (p.Asp3588Gly)
8g.47789048T>GCA371132313PRKDCn.1333A>C
c.3437A>C (p.Asp1146Ala)
c.10760A>C (p.Asp3587Ala)
c.10763A>C (p.Asp3588Ala)
8g.47789049C>ACA371132314PRKDCn.1332G>T
c.3436G>T (p.Asp1146Tyr)
c.10759G>T (p.Asp3587Tyr)
c.10762G>T (p.Asp3588Tyr)
8g.47789049C>GCA371132315PRKDCn.1332G>C
c.3436G>C (p.Asp1146His)
c.10759G>C (p.Asp3587His)
c.10762G>C (p.Asp3588His)
8g.47789049C>TCA371132316PRKDCn.1332G>A
c.3436G>A (p.Asp1146Asn)
c.10759G>A (p.Asp3587Asn)
c.10762G>A (p.Asp3588Asn)
8g.47789050C>ACA371132318PRKDCn.1332-1G>T
c.3436-1G>T (n.3436-1G>T)
c.10759-1G>T (n.10759-1G>T)
c.10762-1G>T (n.10762-1G>T)
8g.47789050C>GCA371132319PRKDCn.1332-1G>C
c.3436-1G>C (n.3436-1G>C)
c.10759-1G>C (n.10759-1G>C)
c.10762-1G>C (n.10762-1G>C)
8g.47789050C>TCA371132317PRKDCn.1332-1G>A
c.3436-1G>A (n.3436-1G>A)
c.10759-1G>A (n.10759-1G>A)
c.10762-1G>A (n.10762-1G>A)
8g.47789050_47789059delCA2687196553PRKDCn.1332-10_1332-1del
c.3436-10_3436-1del (n.3436-10_3436-1del)
c.10759-10_10759-1del (n.10759-10_10759-1del)
c.10762-10_10762-1del (n.10762-10_10762-1del)
 gnomAD v4
8g.47789051T>ACA371132322PRKDCn.1332-2A>T
c.3436-2A>T (n.3436-2A>T)
c.10759-2A>T (n.10759-2A>T)
c.10762-2A>T (n.10762-2A>T)
8g.47789051T>CCA371132320PRKDCn.1332-2A>G
c.3436-2A>G (n.3436-2A>G)
c.10759-2A>G (n.10759-2A>G)
c.10762-2A>G (n.10762-2A>G)
8g.47789051T>GCA371132321PRKDCn.1332-2A>C
c.3436-2A>C (n.3436-2A>C)
c.10759-2A>C (n.10759-2A>C)
c.10762-2A>C (n.10762-2A>C)
8g.47789052G>ACA2687196556PRKDCn.1332-3C>T
c.3436-3C>T (n.3436-3C>T)
c.10759-3C>T (n.10759-3C>T)
c.10762-3C>T (n.10762-3C>T)
 gnomAD v4

Number of alleles fetched