Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.80202243T>ACA357395207PRDM8c.781T>A (p.Phe261Ile)
c.784T>A (p.Phe262Ile)
c.1624T>A (p.Phe542Ile)
c.1621T>A (p.Phe541Ile)
c.1483T>A (p.Phe495Ile)
c.1336T>A (p.Phe446Ile)
c.1198T>A (p.Phe400Ile)
c.1177T>A (p.Phe393Ile)
c.1333T>A (p.Phe445Ile)
c.1420T>A (p.Phe474Ile)
4g.80202243T>CCA279633PRDM8c.781T>C (p.Phe261Leu)
c.784T>C (p.Phe262Leu)
c.1624T>C (p.Phe542Leu)
c.1621T>C (p.Phe541Leu)
c.1483T>C (p.Phe495Leu)
c.1336T>C (p.Phe446Leu)
c.1198T>C (p.Phe400Leu)
c.1177T>C (p.Phe393Leu)
c.1333T>C (p.Phe445Leu)
c.1420T>C (p.Phe474Leu)
ClinVar dbSNP
4g.80202243T>GCA357395208PRDM8c.781T>G (p.Phe261Val)
c.784T>G (p.Phe262Val)
c.1624T>G (p.Phe542Val)
c.1621T>G (p.Phe541Val)
c.1483T>G (p.Phe495Val)
c.1336T>G (p.Phe446Val)
c.1198T>G (p.Phe400Val)
c.1177T>G (p.Phe393Val)
c.1333T>G (p.Phe445Val)
c.1420T>G (p.Phe474Val)
4g.80202243T=CA1471292653PRDM8c.781T= (p.Phe261=)
c.784T= (p.Phe262=)
c.1624T= (p.Phe542=)
c.1621T= (p.Phe541=)
c.1483T= (p.Phe495=)
c.1336T= (p.Phe446=)
c.1198T= (p.Phe400=)
c.1177T= (p.Phe393=)
c.1333T= (p.Phe445=)
c.1420T= (p.Phe474=)
4g.80202244T>ACA357395209PRDM8c.782T>A (p.Phe261Tyr)
c.785T>A (p.Phe262Tyr)
c.1625T>A (p.Phe542Tyr)
c.1622T>A (p.Phe541Tyr)
c.1484T>A (p.Phe495Tyr)
c.1337T>A (p.Phe446Tyr)
c.1199T>A (p.Phe400Tyr)
c.1178T>A (p.Phe393Tyr)
c.1334T>A (p.Phe445Tyr)
c.1421T>A (p.Phe474Tyr)
4g.80202244T>CCA357395210PRDM8c.782T>C (p.Phe261Ser)
c.785T>C (p.Phe262Ser)
c.1625T>C (p.Phe542Ser)
c.1622T>C (p.Phe541Ser)
c.1484T>C (p.Phe495Ser)
c.1337T>C (p.Phe446Ser)
c.1199T>C (p.Phe400Ser)
c.1178T>C (p.Phe393Ser)
c.1334T>C (p.Phe445Ser)
c.1421T>C (p.Phe474Ser)
4g.80202244T>GCA357395211PRDM8c.782T>G (p.Phe261Cys)
c.785T>G (p.Phe262Cys)
c.1625T>G (p.Phe542Cys)
c.1622T>G (p.Phe541Cys)
c.1484T>G (p.Phe495Cys)
c.1337T>G (p.Phe446Cys)
c.1199T>G (p.Phe400Cys)
c.1178T>G (p.Phe393Cys)
c.1334T>G (p.Phe445Cys)
c.1421T>G (p.Phe474Cys)
4g.80202245C>ACA357395212PRDM8c.783C>A (p.Phe261Leu)
c.786C>A (p.Phe262Leu)
c.1626C>A (p.Phe542Leu)
c.1623C>A (p.Phe541Leu)
c.1485C>A (p.Phe495Leu)
c.1338C>A (p.Phe446Leu)
c.1200C>A (p.Phe400Leu)
c.1179C>A (p.Phe393Leu)
c.1335C>A (p.Phe445Leu)
c.1422C>A (p.Phe474Leu)
4g.80202245C>GCA357395213PRDM8c.783C>G (p.Phe261Leu)
c.786C>G (p.Phe262Leu)
c.1626C>G (p.Phe542Leu)
c.1623C>G (p.Phe541Leu)
c.1485C>G (p.Phe495Leu)
c.1338C>G (p.Phe446Leu)
c.1200C>G (p.Phe400Leu)
c.1179C>G (p.Phe393Leu)
c.1335C>G (p.Phe445Leu)
c.1422C>G (p.Phe474Leu)
4g.80202245C>TCA440226855PRDM8c.783C>T (p.Phe261=)
c.786C>T (p.Phe262=)
c.1626C>T (p.Phe542=)
c.1623C>T (p.Phe541=)
c.1485C>T (p.Phe495=)
c.1338C>T (p.Phe446=)
c.1200C>T (p.Phe400=)
c.1179C>T (p.Phe393=)
c.1335C>T (p.Phe445=)
c.1422C>T (p.Phe474=)
COSMIC
4g.80202246C>ACA357395214PRDM8c.784C>A (p.His262Asn)
c.787C>A (p.His263Asn)
c.1627C>A (p.His543Asn)
c.1624C>A (p.His542Asn)
c.1486C>A (p.His496Asn)
c.1339C>A (p.His447Asn)
c.1201C>A (p.His401Asn)
c.1180C>A (p.His394Asn)
c.1336C>A (p.His446Asn)
c.1423C>A (p.His475Asn)
4g.80202246C>GCA357395215PRDM8c.784C>G (p.His262Asp)
c.787C>G (p.His263Asp)
c.1627C>G (p.His543Asp)
c.1624C>G (p.His542Asp)
c.1486C>G (p.His496Asp)
c.1339C>G (p.His447Asp)
c.1201C>G (p.His401Asp)
c.1180C>G (p.His394Asp)
c.1336C>G (p.His446Asp)
c.1423C>G (p.His475Asp)
4g.80202246C>TCA357395216PRDM8c.784C>T (p.His262Tyr)
c.787C>T (p.His263Tyr)
c.1627C>T (p.His543Tyr)
c.1624C>T (p.His542Tyr)
c.1486C>T (p.His496Tyr)
c.1339C>T (p.His447Tyr)
c.1201C>T (p.His401Tyr)
c.1180C>T (p.His394Tyr)
c.1336C>T (p.His446Tyr)
c.1423C>T (p.His475Tyr)
4g.80202247A>CCA357395217PRDM8c.785A>C (p.His262Pro)
c.788A>C (p.His263Pro)
c.1628A>C (p.His543Pro)
c.1625A>C (p.His542Pro)
c.1487A>C (p.His496Pro)
c.1340A>C (p.His447Pro)
c.1202A>C (p.His401Pro)
c.1181A>C (p.His394Pro)
c.1337A>C (p.His446Pro)
c.1424A>C (p.His475Pro)
4g.80202247A>GCA357395218PRDM8c.785A>G (p.His262Arg)
c.788A>G (p.His263Arg)
c.1628A>G (p.His543Arg)
c.1625A>G (p.His542Arg)
c.1487A>G (p.His496Arg)
c.1340A>G (p.His447Arg)
c.1202A>G (p.His401Arg)
c.1181A>G (p.His394Arg)
c.1337A>G (p.His446Arg)
c.1424A>G (p.His475Arg)
4g.80202247A>TCA357395219PRDM8c.785A>T (p.His262Leu)
c.788A>T (p.His263Leu)
c.1628A>T (p.His543Leu)
c.1625A>T (p.His542Leu)
c.1487A>T (p.His496Leu)
c.1340A>T (p.His447Leu)
c.1202A>T (p.His401Leu)
c.1181A>T (p.His394Leu)
c.1337A>T (p.His446Leu)
c.1424A>T (p.His475Leu)
4g.80202248C>ACA357395220PRDM8c.786C>A (p.His262Gln)
c.789C>A (p.His263Gln)
c.1629C>A (p.His543Gln)
c.1626C>A (p.His542Gln)
c.1488C>A (p.His496Gln)
c.1341C>A (p.His447Gln)
c.1203C>A (p.His401Gln)
c.1182C>A (p.His394Gln)
c.1338C>A (p.His446Gln)
c.1425C>A (p.His475Gln)
4g.80202248C>GCA357395221PRDM8c.786C>G (p.His262Gln)
c.789C>G (p.His263Gln)
c.1629C>G (p.His543Gln)
c.1626C>G (p.His542Gln)
c.1488C>G (p.His496Gln)
c.1341C>G (p.His447Gln)
c.1203C>G (p.His401Gln)
c.1182C>G (p.His394Gln)
c.1338C>G (p.His446Gln)
c.1425C>G (p.His475Gln)
4g.80202248C>TCA440226861PRDM8c.786C>T (p.His262=)
c.789C>T (p.His263=)
c.1629C>T (p.His543=)
c.1626C>T (p.His542=)
c.1488C>T (p.His496=)
c.1341C>T (p.His447=)
c.1203C>T (p.His401=)
c.1182C>T (p.His394=)
c.1338C>T (p.His446=)
c.1425C>T (p.His475=)
gnomAD v4
4g.80202249A>CCA357395222PRDM8c.787A>C (p.Asn263His)
c.790A>C (p.Asn264His)
c.1630A>C (p.Asn544His)
c.1627A>C (p.Asn543His)
c.1489A>C (p.Asn497His)
c.1342A>C (p.Asn448His)
c.1204A>C (p.Asn402His)
c.1183A>C (p.Asn395His)
c.1339A>C (p.Asn447His)
c.1426A>C (p.Asn476His)
4g.80202249A>GCA357395223PRDM8c.787A>G (p.Asn263Asp)
c.790A>G (p.Asn264Asp)
c.1630A>G (p.Asn544Asp)
c.1627A>G (p.Asn543Asp)
c.1489A>G (p.Asn497Asp)
c.1342A>G (p.Asn448Asp)
c.1204A>G (p.Asn402Asp)
c.1183A>G (p.Asn395Asp)
c.1339A>G (p.Asn447Asp)
c.1426A>G (p.Asn476Asp)
4g.80202249A>TCA357395224PRDM8c.787A>T (p.Asn263Tyr)
c.790A>T (p.Asn264Tyr)
c.1630A>T (p.Asn544Tyr)
c.1627A>T (p.Asn543Tyr)
c.1489A>T (p.Asn497Tyr)
c.1342A>T (p.Asn448Tyr)
c.1204A>T (p.Asn402Tyr)
c.1183A>T (p.Asn395Tyr)
c.1339A>T (p.Asn447Tyr)
c.1426A>T (p.Asn476Tyr)
4g.80202250A>CCA357395225PRDM8c.788A>C (p.Asn263Thr)
c.791A>C (p.Asn264Thr)
c.1631A>C (p.Asn544Thr)
c.1628A>C (p.Asn543Thr)
c.1490A>C (p.Asn497Thr)
c.1343A>C (p.Asn448Thr)
c.1205A>C (p.Asn402Thr)
c.1184A>C (p.Asn395Thr)
c.1340A>C (p.Asn447Thr)
c.1427A>C (p.Asn476Thr)
4g.80202250A>GCA357395226PRDM8c.788A>G (p.Asn263Ser)
c.791A>G (p.Asn264Ser)
c.1631A>G (p.Asn544Ser)
c.1628A>G (p.Asn543Ser)
c.1490A>G (p.Asn497Ser)
c.1343A>G (p.Asn448Ser)
c.1205A>G (p.Asn402Ser)
c.1184A>G (p.Asn395Ser)
c.1340A>G (p.Asn447Ser)
c.1427A>G (p.Asn476Ser)
4g.80202250A>TCA357395227PRDM8c.788A>T (p.Asn263Ile)
c.791A>T (p.Asn264Ile)
c.1631A>T (p.Asn544Ile)
c.1628A>T (p.Asn543Ile)
c.1490A>T (p.Asn497Ile)
c.1343A>T (p.Asn448Ile)
c.1205A>T (p.Asn402Ile)
c.1184A>T (p.Asn395Ile)
c.1340A>T (p.Asn447Ile)
c.1427A>T (p.Asn476Ile)
4g.80202251C>ACA357395228PRDM8c.789C>A (p.Asn263Lys)
c.792C>A (p.Asn264Lys)
c.1632C>A (p.Asn544Lys)
c.1629C>A (p.Asn543Lys)
c.1491C>A (p.Asn497Lys)
c.1344C>A (p.Asn448Lys)
c.1206C>A (p.Asn402Lys)
c.1185C>A (p.Asn395Lys)
c.1341C>A (p.Asn447Lys)
c.1428C>A (p.Asn476Lys)
4g.80202251C=CA1471292658PRDM8c.789C= (p.Asn263=)
c.792C= (p.Asn264=)
c.1632C= (p.Asn544=)
c.1629C= (p.Asn543=)
c.1491C= (p.Asn497=)
c.1344C= (p.Asn448=)
c.1206C= (p.Asn402=)
c.1185C= (p.Asn395=)
c.1341C= (p.Asn447=)
c.1428C= (p.Asn476=)
4g.80202251C>GCA357395229PRDM8c.789C>G (p.Asn263Lys)
c.792C>G (p.Asn264Lys)
c.1632C>G (p.Asn544Lys)
c.1629C>G (p.Asn543Lys)
c.1491C>G (p.Asn497Lys)
c.1344C>G (p.Asn448Lys)
c.1206C>G (p.Asn402Lys)
c.1185C>G (p.Asn395Lys)
c.1341C>G (p.Asn447Lys)
c.1428C>G (p.Asn476Lys)
4g.80202251C>TCA440226868PRDM8c.789C>T (p.Asn263=)
c.792C>T (p.Asn264=)
c.1632C>T (p.Asn544=)
c.1629C>T (p.Asn543=)
c.1491C>T (p.Asn497=)
c.1344C>T (p.Asn448=)
c.1206C>T (p.Asn402=)
c.1185C>T (p.Asn395=)
c.1341C>T (p.Asn447=)
c.1428C>T (p.Asn476=)
dbSNP gnomAD v3 gnomAD v4
4g.80202252C>ACA357395230PRDM8c.790C>A (p.Leu264Met)
c.793C>A (p.Leu265Met)
c.1633C>A (p.Leu545Met)
c.1630C>A (p.Leu544Met)
c.1492C>A (p.Leu498Met)
c.1345C>A (p.Leu449Met)
c.1207C>A (p.Leu403Met)
c.1186C>A (p.Leu396Met)
c.1342C>A (p.Leu448Met)
c.1429C>A (p.Leu477Met)
4g.80202252C>GCA357395231PRDM8c.790C>G (p.Leu264Val)
c.793C>G (p.Leu265Val)
c.1633C>G (p.Leu545Val)
c.1630C>G (p.Leu544Val)
c.1492C>G (p.Leu498Val)
c.1345C>G (p.Leu449Val)
c.1207C>G (p.Leu403Val)
c.1186C>G (p.Leu396Val)
c.1342C>G (p.Leu448Val)
c.1429C>G (p.Leu477Val)
4g.80202252C>TCA440226873PRDM8c.790C>T (p.Leu264=)
c.793C>T (p.Leu265=)
c.1633C>T (p.Leu545=)
c.1630C>T (p.Leu544=)
c.1492C>T (p.Leu498=)
c.1345C>T (p.Leu449=)
c.1207C>T (p.Leu403=)
c.1186C>T (p.Leu396=)
c.1342C>T (p.Leu448=)
c.1429C>T (p.Leu477=)
4g.80202253T>ACA357395232PRDM8c.791T>A (p.Leu264Gln)
c.794T>A (p.Leu265Gln)
c.1634T>A (p.Leu545Gln)
c.1631T>A (p.Leu544Gln)
c.1493T>A (p.Leu498Gln)
c.1346T>A (p.Leu449Gln)
c.1208T>A (p.Leu403Gln)
c.1187T>A (p.Leu396Gln)
c.1343T>A (p.Leu448Gln)
c.1430T>A (p.Leu477Gln)
4g.80202253T>CCA357395233PRDM8c.791T>C (p.Leu264Pro)
c.794T>C (p.Leu265Pro)
c.1634T>C (p.Leu545Pro)
c.1631T>C (p.Leu544Pro)
c.1493T>C (p.Leu498Pro)
c.1346T>C (p.Leu449Pro)
c.1208T>C (p.Leu403Pro)
c.1187T>C (p.Leu396Pro)
c.1343T>C (p.Leu448Pro)
c.1430T>C (p.Leu477Pro)
gnomAD v4
4g.80202253T>GCA357395234PRDM8c.791T>G (p.Leu264Arg)
c.794T>G (p.Leu265Arg)
c.1634T>G (p.Leu545Arg)
c.1631T>G (p.Leu544Arg)
c.1493T>G (p.Leu498Arg)
c.1346T>G (p.Leu449Arg)
c.1208T>G (p.Leu403Arg)
c.1187T>G (p.Leu396Arg)
c.1343T>G (p.Leu448Arg)
c.1430T>G (p.Leu477Arg)
4g.80202254G>ACA440226877PRDM8c.792G>A (p.Leu264=)
c.795G>A (p.Leu265=)
c.1635G>A (p.Leu545=)
c.1632G>A (p.Leu544=)
c.1494G>A (p.Leu498=)
c.1347G>A (p.Leu449=)
c.1209G>A (p.Leu403=)
c.1188G>A (p.Leu396=)
c.1344G>A (p.Leu448=)
c.1431G>A (p.Leu477=)
4g.80202254G>CCA440226880PRDM8c.792G>C (p.Leu264=)
c.795G>C (p.Leu265=)
c.1635G>C (p.Leu545=)
c.1632G>C (p.Leu544=)
c.1494G>C (p.Leu498=)
c.1347G>C (p.Leu449=)
c.1209G>C (p.Leu403=)
c.1188G>C (p.Leu396=)
c.1344G>C (p.Leu448=)
c.1431G>C (p.Leu477=)
4g.80202254G>TCA440226878PRDM8c.792G>T (p.Leu264=)
c.795G>T (p.Leu265=)
c.1635G>T (p.Leu545=)
c.1632G>T (p.Leu544=)
c.1494G>T (p.Leu498=)
c.1347G>T (p.Leu449=)
c.1209G>T (p.Leu403=)
c.1188G>T (p.Leu396=)
c.1344G>T (p.Leu448=)
c.1431G>T (p.Leu477=)
gnomAD v4
4g.80202255G>ACA357395236PRDM8c.793G>A (p.Ala265Thr)
c.796G>A (p.Ala266Thr)
c.1636G>A (p.Ala546Thr)
c.1633G>A (p.Ala545Thr)
c.1495G>A (p.Ala499Thr)
c.1348G>A (p.Ala450Thr)
c.1210G>A (p.Ala404Thr)
c.1189G>A (p.Ala397Thr)
c.1345G>A (p.Ala449Thr)
c.1432G>A (p.Ala478Thr)
4g.80202255G>CCA357395237PRDM8c.793G>C (p.Ala265Pro)
c.796G>C (p.Ala266Pro)
c.1636G>C (p.Ala546Pro)
c.1633G>C (p.Ala545Pro)
c.1495G>C (p.Ala499Pro)
c.1348G>C (p.Ala450Pro)
c.1210G>C (p.Ala404Pro)
c.1189G>C (p.Ala397Pro)
c.1345G>C (p.Ala449Pro)
c.1432G>C (p.Ala478Pro)
4g.80202255G>TCA357395235PRDM8c.793G>T (p.Ala265Ser)
c.796G>T (p.Ala266Ser)
c.1636G>T (p.Ala546Ser)
c.1633G>T (p.Ala545Ser)
c.1495G>T (p.Ala499Ser)
c.1348G>T (p.Ala450Ser)
c.1210G>T (p.Ala404Ser)
c.1189G>T (p.Ala397Ser)
c.1345G>T (p.Ala449Ser)
c.1432G>T (p.Ala478Ser)
4g.80202256C>ACA357395239PRDM8c.794C>A (p.Ala265Asp)
c.797C>A (p.Ala266Asp)
c.1637C>A (p.Ala546Asp)
c.1634C>A (p.Ala545Asp)
c.1496C>A (p.Ala499Asp)
c.1349C>A (p.Ala450Asp)
c.1211C>A (p.Ala404Asp)
c.1190C>A (p.Ala397Asp)
c.1346C>A (p.Ala449Asp)
c.1433C>A (p.Ala478Asp)
4g.80202256C>GCA357395238PRDM8c.794C>G (p.Ala265Gly)
c.797C>G (p.Ala266Gly)
c.1637C>G (p.Ala546Gly)
c.1634C>G (p.Ala545Gly)
c.1496C>G (p.Ala499Gly)
c.1349C>G (p.Ala450Gly)
c.1211C>G (p.Ala404Gly)
c.1190C>G (p.Ala397Gly)
c.1346C>G (p.Ala449Gly)
c.1433C>G (p.Ala478Gly)
4g.80202256C>TCA357395240PRDM8c.794C>T (p.Ala265Val)
c.797C>T (p.Ala266Val)
c.1637C>T (p.Ala546Val)
c.1634C>T (p.Ala545Val)
c.1496C>T (p.Ala499Val)
c.1349C>T (p.Ala450Val)
c.1211C>T (p.Ala404Val)
c.1190C>T (p.Ala397Val)
c.1346C>T (p.Ala449Val)
c.1433C>T (p.Ala478Val)
4g.80202257C>ACA440226889PRDM8c.795C>A (p.Ala265=)
c.798C>A (p.Ala266=)
c.1638C>A (p.Ala546=)
c.1635C>A (p.Ala545=)
c.1497C>A (p.Ala499=)
c.1350C>A (p.Ala450=)
c.1212C>A (p.Ala404=)
c.1191C>A (p.Ala397=)
c.1347C>A (p.Ala449=)
c.1434C>A (p.Ala478=)
4g.80202257C=CA1471292661PRDM8c.795C= (p.Ala265=)
c.798C= (p.Ala266=)
c.1638C= (p.Ala546=)
c.1635C= (p.Ala545=)
c.1497C= (p.Ala499=)
c.1350C= (p.Ala450=)
c.1212C= (p.Ala404=)
c.1191C= (p.Ala397=)
c.1347C= (p.Ala449=)
c.1434C= (p.Ala478=)
4g.80202257C>GCA2982325PRDM8c.795C>G (p.Ala265=)
c.798C>G (p.Ala266=)
c.1638C>G (p.Ala546=)
c.1635C>G (p.Ala545=)
c.1497C>G (p.Ala499=)
c.1350C>G (p.Ala450=)
c.1212C>G (p.Ala404=)
c.1191C>G (p.Ala397=)
c.1347C>G (p.Ala449=)
c.1434C>G (p.Ala478=)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.80202257C>TCA2982326PRDM8c.795C>T (p.Ala265=)
c.798C>T (p.Ala266=)
c.1638C>T (p.Ala546=)
c.1635C>T (p.Ala545=)
c.1497C>T (p.Ala499=)
c.1350C>T (p.Ala450=)
c.1212C>T (p.Ala404=)
c.1191C>T (p.Ala397=)
c.1347C>T (p.Ala449=)
c.1434C>T (p.Ala478=)
dbSNP ExAC gnomAD v2 gnomAD v4
4g.80202258A>CCA440226891PRDM8c.796A>C (p.Arg266=)
c.799A>C (p.Arg267=)
c.1639A>C (p.Arg547=)
c.1636A>C (p.Arg546=)
c.1498A>C (p.Arg500=)
c.1351A>C (p.Arg451=)
c.1213A>C (p.Arg405=)
c.1192A>C (p.Arg398=)
c.1348A>C (p.Arg450=)
c.1435A>C (p.Arg479=)
gnomAD v4
4g.80202258A>GCA357395241PRDM8c.796A>G (p.Arg266Gly)
c.799A>G (p.Arg267Gly)
c.1639A>G (p.Arg547Gly)
c.1636A>G (p.Arg546Gly)
c.1498A>G (p.Arg500Gly)
c.1351A>G (p.Arg451Gly)
c.1213A>G (p.Arg405Gly)
c.1192A>G (p.Arg398Gly)
c.1348A>G (p.Arg450Gly)
c.1435A>G (p.Arg479Gly)

Number of alleles fetched