Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.29672739G>ACA363043353ZFP57c.1372C>T (p.His458Tyr)
c.1156C>T (p.His386Tyr)
c.1120C>T (p.His374Tyr)
c.1312C>T (p.His438Tyr)
6g.29672739G>CCA251581ZFP57c.1372C>G (p.His458Asp)
c.1156C>G (p.His386Asp)
c.1120C>G (p.His374Asp)
c.1312C>G (p.His438Asp)
ClinVar dbSNP
6g.29672739G=CA1618398862ZFP57c.1372C= (p.His458=)
c.1156C= (p.His386=)
c.1120C= (p.His374=)
c.1312C= (p.His438=)
6g.29672739G>TCA363043352ZFP57c.1372C>A (p.His458Asn)
c.1156C>A (p.His386Asn)
c.1120C>A (p.His374Asn)
c.1312C>A (p.His438Asn)
dbSNP gnomAD v4
6g.29672740A>CCA363043354ZFP57c.1371T>G (p.Asp457Glu)
c.1155T>G (p.Asp385Glu)
c.1119T>G (p.Asp373Glu)
c.1311T>G (p.Asp437Glu)
6g.29672740A>GCA449458328ZFP57c.1371T>C (p.Asp457=)
c.1155T>C (p.Asp385=)
c.1119T>C (p.Asp373=)
c.1311T>C (p.Asp437=)
6g.29672740A>TCA363043355ZFP57c.1371T>A (p.Asp457Glu)
c.1155T>A (p.Asp385Glu)
c.1119T>A (p.Asp373Glu)
c.1311T>A (p.Asp437Glu)
6g.29672741T>ACA363043356ZFP57c.1370A>T (p.Asp457Val)
c.1154A>T (p.Asp385Val)
c.1118A>T (p.Asp373Val)
c.1310A>T (p.Asp437Val)
6g.29672741T>CCA363043357ZFP57c.1370A>G (p.Asp457Gly)
c.1154A>G (p.Asp385Gly)
c.1118A>G (p.Asp373Gly)
c.1310A>G (p.Asp437Gly)
dbSNP gnomAD v3 gnomAD v4
6g.29672741T>GCA363043358ZFP57c.1370A>C (p.Asp457Ala)
c.1154A>C (p.Asp385Ala)
c.1118A>C (p.Asp373Ala)
c.1310A>C (p.Asp437Ala)
6g.29672741T=CA1618398863ZFP57c.1370A= (p.Asp457=)
c.1154A= (p.Asp385=)
c.1118A= (p.Asp373=)
c.1310A= (p.Asp437=)
6g.29672742C>ACA363043359ZFP57c.1369G>T (p.Asp457Tyr)
c.1153G>T (p.Asp385Tyr)
c.1117G>T (p.Asp373Tyr)
c.1309G>T (p.Asp437Tyr)
6g.29672742C>GCA363043360ZFP57c.1369G>C (p.Asp457His)
c.1153G>C (p.Asp385His)
c.1117G>C (p.Asp373His)
c.1309G>C (p.Asp437His)
6g.29672742C>TCA363043361ZFP57c.1369G>A (p.Asp457Asn)
c.1153G>A (p.Asp385Asn)
c.1117G>A (p.Asp373Asn)
c.1309G>A (p.Asp437Asn)
6g.29672743C>ACA363043362ZFP57c.1368G>T (p.Met456Ile)
c.1152G>T (p.Met384Ile)
c.1116G>T (p.Met372Ile)
c.1308G>T (p.Met436Ile)
6g.29672743C>GCA363043363ZFP57c.1368G>C (p.Met456Ile)
c.1152G>C (p.Met384Ile)
c.1116G>C (p.Met372Ile)
c.1308G>C (p.Met436Ile)
6g.29672743C>TCA363043364ZFP57c.1368G>A (p.Met456Ile)
c.1152G>A (p.Met384Ile)
c.1116G>A (p.Met372Ile)
c.1308G>A (p.Met436Ile)
6g.29672744A>CCA363043367ZFP57c.1367T>G (p.Met456Arg)
c.1151T>G (p.Met384Arg)
c.1115T>G (p.Met372Arg)
c.1307T>G (p.Met436Arg)
6g.29672744A>GCA363043366ZFP57c.1367T>C (p.Met456Thr)
c.1151T>C (p.Met384Thr)
c.1115T>C (p.Met372Thr)
c.1307T>C (p.Met436Thr)
6g.29672744A>TCA363043365ZFP57c.1367T>A (p.Met456Lys)
c.1151T>A (p.Met384Lys)
c.1115T>A (p.Met372Lys)
c.1307T>A (p.Met436Lys)
6g.29672745T>ACA363043368ZFP57c.1366A>T (p.Met456Leu)
c.1150A>T (p.Met384Leu)
c.1114A>T (p.Met372Leu)
c.1306A>T (p.Met436Leu)
dbSNP gnomAD v3 gnomAD v4
6g.29672745T>CCA363043369ZFP57c.1366A>G (p.Met456Val)
c.1150A>G (p.Met384Val)
c.1114A>G (p.Met372Val)
c.1306A>G (p.Met436Val)
dbSNP
6g.29672745T>GCA363043370ZFP57c.1366A>C (p.Met456Leu)
c.1150A>C (p.Met384Leu)
c.1114A>C (p.Met372Leu)
c.1306A>C (p.Met436Leu)
6g.29672745T=CA1618398864ZFP57c.1366A= (p.Met456=)
c.1150A= (p.Met384=)
c.1114A= (p.Met372=)
c.1306A= (p.Met436=)
6g.29672746A>CCA449458330ZFP57c.1365T>G (p.Leu455=)
c.1149T>G (p.Leu383=)
c.1113T>G (p.Leu371=)
c.1305T>G (p.Leu435=)
6g.29672746A>GCA449458332ZFP57c.1365T>C (p.Leu455=)
c.1149T>C (p.Leu383=)
c.1113T>C (p.Leu371=)
c.1305T>C (p.Leu435=)
6g.29672746A>TCA449458331ZFP57c.1365T>A (p.Leu455=)
c.1149T>A (p.Leu383=)
c.1113T>A (p.Leu371=)
c.1305T>A (p.Leu435=)
6g.29672747A>CCA363043371ZFP57c.1364T>G (p.Leu455Arg)
c.1148T>G (p.Leu383Arg)
c.1112T>G (p.Leu371Arg)
c.1304T>G (p.Leu435Arg)
6g.29672747A>GCA363043372ZFP57c.1364T>C (p.Leu455Pro)
c.1148T>C (p.Leu383Pro)
c.1112T>C (p.Leu371Pro)
c.1304T>C (p.Leu435Pro)
6g.29672747A>TCA363043373ZFP57c.1364T>A (p.Leu455His)
c.1148T>A (p.Leu383His)
c.1112T>A (p.Leu371His)
c.1304T>A (p.Leu435His)
6g.29672748G>ACA363043374ZFP57c.1363C>T (p.Leu455Phe)
c.1147C>T (p.Leu383Phe)
c.1111C>T (p.Leu371Phe)
c.1303C>T (p.Leu435Phe)
dbSNP
6g.29672748G>CCA363043375ZFP57c.1363C>G (p.Leu455Val)
c.1147C>G (p.Leu383Val)
c.1111C>G (p.Leu371Val)
c.1303C>G (p.Leu435Val)
6g.29672748G=CA1618398865ZFP57c.1363C= (p.Leu455=)
c.1147C= (p.Leu383=)
c.1111C= (p.Leu371=)
c.1303C= (p.Leu435=)
6g.29672748G>TCA363043376ZFP57c.1363C>A (p.Leu455Ile)
c.1147C>A (p.Leu383Ile)
c.1111C>A (p.Leu371Ile)
c.1303C>A (p.Leu435Ile)
6g.29672749G>ACA449458335ZFP57c.1362C>T (p.Gly454=)
c.1146C>T (p.Gly382=)
c.1110C>T (p.Gly370=)
c.1302C>T (p.Gly434=)
6g.29672749G>CCA449458333ZFP57c.1362C>G (p.Gly454=)
c.1146C>G (p.Gly382=)
c.1110C>G (p.Gly370=)
c.1302C>G (p.Gly434=)
6g.29672749G>TCA449458334ZFP57c.1362C>A (p.Gly454=)
c.1146C>A (p.Gly382=)
c.1110C>A (p.Gly370=)
c.1302C>A (p.Gly434=)
6g.29672750C>ACA363043377ZFP57c.1361G>T (p.Gly454Val)
c.1145G>T (p.Gly382Val)
c.1109G>T (p.Gly370Val)
c.1301G>T (p.Gly434Val)
6g.29672750C=CA1618398866ZFP57c.1361G= (p.Gly454=)
c.1145G= (p.Gly382=)
c.1109G= (p.Gly370=)
c.1301G= (p.Gly434=)
6g.29672750C>GCA363043378ZFP57c.1361G>C (p.Gly454Ala)
c.1145G>C (p.Gly382Ala)
c.1109G>C (p.Gly370Ala)
c.1301G>C (p.Gly434Ala)
6g.29672750C>TCA3690687ZFP57c.1361G>A (p.Gly454Asp)
c.1145G>A (p.Gly382Asp)
c.1109G>A (p.Gly370Asp)
c.1301G>A (p.Gly434Asp)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.29672751C>ACA363043380ZFP57c.1360G>T (p.Gly454Cys)
c.1144G>T (p.Gly382Cys)
c.1108G>T (p.Gly370Cys)
c.1300G>T (p.Gly434Cys)
6g.29672751C>GCA363043381ZFP57c.1360G>C (p.Gly454Arg)
c.1144G>C (p.Gly382Arg)
c.1108G>C (p.Gly370Arg)
c.1300G>C (p.Gly434Arg)
6g.29672751C>TCA363043379ZFP57c.1360G>A (p.Gly454Ser)
c.1144G>A (p.Gly382Ser)
c.1108G>A (p.Gly370Ser)
c.1300G>A (p.Gly434Ser)
6g.29672752C>ACA363043383ZFP57c.1359G>T (p.Glu453Asp)
c.1143G>T (p.Glu381Asp)
c.1107G>T (p.Glu369Asp)
c.1299G>T (p.Glu433Asp)
6g.29672752C=CA1618398867ZFP57c.1359G= (p.Glu453=)
c.1143G= (p.Glu381=)
c.1107G= (p.Glu369=)
c.1299G= (p.Glu433=)
6g.29672752C>GCA363043382ZFP57c.1359G>C (p.Glu453Asp)
c.1143G>C (p.Glu381Asp)
c.1107G>C (p.Glu369Asp)
c.1299G>C (p.Glu433Asp)
6g.29672752C>TCA3690688ZFP57c.1359G>A (p.Glu453=)
c.1143G>A (p.Glu381=)
c.1107G>A (p.Glu369=)
c.1299G>A (p.Glu433=)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.29672753T>ACA363043384ZFP57c.1358A>T (p.Glu453Val)
c.1142A>T (p.Glu381Val)
c.1106A>T (p.Glu369Val)
c.1298A>T (p.Glu433Val)
6g.29672753T>CCA363043385ZFP57c.1358A>G (p.Glu453Gly)
c.1142A>G (p.Glu381Gly)
c.1106A>G (p.Glu369Gly)
c.1298A>G (p.Glu433Gly)

Number of alleles fetched