Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.47789028C>ACA371132261PRKDCn.1353G>T
c.3457G>T (p.Ala1153Ser)
c.10780G>T (p.Ala3594Ser)
c.10783G>T (p.Ala3595Ser)
8g.47789028C>GCA371132263PRKDCn.1353G>C
c.3457G>C (p.Ala1153Pro)
c.10780G>C (p.Ala3594Pro)
c.10783G>C (p.Ala3595Pro)
8g.47789028C>TCA371132262PRKDCn.1353G>A
c.3457G>A (p.Ala1153Thr)
c.10780G>A (p.Ala3594Thr)
c.10783G>A (p.Ala3595Thr)
8g.47789029T>ACA371132264PRKDCn.1352A>T
c.3456A>T (p.Arg1152Ser)
c.10779A>T (p.Arg3593Ser)
c.10782A>T (p.Arg3594Ser)
8g.47789029T>CCA460603924PRKDCn.1352A>G
c.3456A>G (p.Arg1152=)
c.10779A>G (p.Arg3593=)
c.10782A>G (p.Arg3594=)
8g.47789029T>GCA371132265PRKDCn.1352A>C
c.3456A>C (p.Arg1152Ser)
c.10779A>C (p.Arg3593Ser)
c.10782A>C (p.Arg3594Ser)
8g.47789030C>ACA371132266PRKDCn.1351G>T
c.3455G>T (p.Arg1152Ile)
c.10778G>T (p.Arg3593Ile)
c.10781G>T (p.Arg3594Ile)
8g.47789030C=CA1781813533PRKDCn.1351G=
c.3455G= (p.Arg1152=)
c.10778G= (p.Arg3593=)
c.10781G= (p.Arg3594=)
8g.47789030C>GCA371132267PRKDCn.1351G>C
c.3455G>C (p.Arg1152Thr)
c.10778G>C (p.Arg3593Thr)
c.10781G>C (p.Arg3594Thr)
8g.47789030C>TCA4739238PRKDCn.1351G>A
c.3455G>A (p.Arg1152Lys)
c.10778G>A (p.Arg3593Lys)
c.10781G>A (p.Arg3594Lys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.47789031T>ACA371132268PRKDCn.1350A>T
c.3454A>T (p.Arg1152Ter)
c.10777A>T (p.Arg3593Ter)
c.10780A>T (p.Arg3594Ter)
8g.47789031T>CCA371132269PRKDCn.1350A>G
c.3454A>G (p.Arg1152Gly)
c.10777A>G (p.Arg3593Gly)
c.10780A>G (p.Arg3594Gly)
 dbSNP gnomAD v4
8g.47789031T>GCA460603925PRKDCn.1350A>C
c.3454A>C (p.Arg1152=)
c.10777A>C (p.Arg3593=)
c.10780A>C (p.Arg3594=)
8g.47789031T=CA1781813534PRKDCn.1350A=
c.3454A= (p.Arg1152=)
c.10777A= (p.Arg3593=)
c.10780A= (p.Arg3594=)
8g.47789032T>ACA460603929PRKDCn.1349A>T
c.3453A>T (p.Val1151=)
c.10776A>T (p.Val3592=)
c.10779A>T (p.Val3593=)
8g.47789032T>CCA460603928PRKDCn.1349A>G
c.3453A>G (p.Val1151=)
c.10776A>G (p.Val3592=)
c.10779A>G (p.Val3593=)
8g.47789032T>GCA460603927PRKDCn.1349A>C
c.3453A>C (p.Val1151=)
c.10776A>C (p.Val3592=)
c.10779A>C (p.Val3593=)
8g.47789033A>CCA371132270PRKDCn.1348T>G
c.3452T>G (p.Val1151Gly)
c.10775T>G (p.Val3592Gly)
c.10778T>G (p.Val3593Gly)
8g.47789033A>GCA371132271PRKDCn.1348T>C
c.3452T>C (p.Val1151Ala)
c.10775T>C (p.Val3592Ala)
c.10778T>C (p.Val3593Ala)
8g.47789033A>TCA371132272PRKDCn.1348T>A
c.3452T>A (p.Val1151Glu)
c.10775T>A (p.Val3592Glu)
c.10778T>A (p.Val3593Glu)
8g.47789034C>ACA371132273PRKDCn.1347G>T
c.3451G>T (p.Val1151Leu)
c.10774G>T (p.Val3592Leu)
c.10777G>T (p.Val3593Leu)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.47789034C=CA1781813535PRKDCn.1347G=
c.3451G= (p.Val1151=)
c.10774G= (p.Val3592=)
c.10777G= (p.Val3593=)
8g.47789034C>GCA371132274PRKDCn.1347G>C
c.3451G>C (p.Val1151Leu)
c.10774G>C (p.Val3592Leu)
c.10777G>C (p.Val3593Leu)
8g.47789034C>TCA371132275PRKDCn.1347G>A
c.3451G>A (p.Val1151Ile)
c.10774G>A (p.Val3592Ile)
c.10777G>A (p.Val3593Ile)
 dbSNP gnomAD v2 gnomAD v4
8g.47789035A=CA1781813536PRKDCn.1346T=
c.3450T= (p.Asp1150=)
c.10773T= (p.Asp3591=)
c.10776T= (p.Asp3592=)
8g.47789035A>CCA371132277PRKDCn.1346T>G
c.3450T>G (p.Asp1150Glu)
c.10773T>G (p.Asp3591Glu)
c.10776T>G (p.Asp3592Glu)
8g.47789035A>GCA4739239PRKDCn.1346T>C
c.3450T>C (p.Asp1150=)
c.10773T>C (p.Asp3591=)
c.10776T>C (p.Asp3592=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
8g.47789035A>TCA371132276PRKDCn.1346T>A
c.3450T>A (p.Asp1150Glu)
c.10773T>A (p.Asp3591Glu)
c.10776T>A (p.Asp3592Glu)
8g.47789036T>ACA371132278PRKDCn.1345A>T
c.3449A>T (p.Asp1150Val)
c.10772A>T (p.Asp3591Val)
c.10775A>T (p.Asp3592Val)
8g.47789036T>CCA371132279PRKDCn.1345A>G
c.3449A>G (p.Asp1150Gly)
c.10772A>G (p.Asp3591Gly)
c.10775A>G (p.Asp3592Gly)
 gnomAD v4
8g.47789036T>GCA371132280PRKDCn.1345A>C
c.3449A>C (p.Asp1150Ala)
c.10772A>C (p.Asp3591Ala)
c.10775A>C (p.Asp3592Ala)
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

Number of alleles fetched