UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 1 | g.114677917A= | CA1145430801 | AMPD1 | c.1205T= (p.Ile402=) c.1217T= (p.Ile406=) c.1000T= (n.1000T=) n.882T= c.1304T= (p.Ile435=) c.1316T= (p.Ile439=) | |
| 1 | g.114677917A>C | CA341748958 | AMPD1 | c.1205T>G (p.Ile402Ser) c.1217T>G (p.Ile406Ser) c.1000T>G (n.1000T>G) n.882T>G c.1304T>G (p.Ile435Ser) c.1316T>G (p.Ile439Ser) | |
| 1 | g.114677917A>G | CA1020189 | AMPD1 | c.1205T>C (p.Ile402Thr) c.1217T>C (p.Ile406Thr) c.1000T>C (n.1000T>C) n.882T>C c.1304T>C (p.Ile435Thr) c.1316T>C (p.Ile439Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.114677917A>T | CA341748957 | AMPD1 | c.1205T>A (p.Ile402Asn) c.1217T>A (p.Ile406Asn) c.1000T>A (n.1000T>A) n.882T>A c.1304T>A (p.Ile435Asn) c.1316T>A (p.Ile439Asn) | |
| 1 | g.114677918T>A | CA341748959 | AMPD1 | c.1204A>T (p.Ile402Phe) c.1216A>T (p.Ile406Phe) c.999A>T (n.999A>T) n.881A>T c.1303A>T (p.Ile435Phe) c.1315A>T (p.Ile439Phe) | dbSNP gnomAD v3 gnomAD v4 |
| 1 | g.114677918T>C | CA341748960 | AMPD1 | c.1204A>G (p.Ile402Val) c.1216A>G (p.Ile406Val) c.999A>G (n.999A>G) n.881A>G c.1303A>G (p.Ile435Val) c.1315A>G (p.Ile439Val) | COSMIC COSMIC |
| 1 | g.114677918T>G | CA341748961 | AMPD1 | c.1204A>C (p.Ile402Leu) c.1216A>C (p.Ile406Leu) c.999A>C (n.999A>C) n.881A>C c.1303A>C (p.Ile435Leu) c.1315A>C (p.Ile439Leu) | |
| 1 | g.114677918T= | CA1190276593 | AMPD1 | c.1204A= (p.Ile402=) c.1216A= (p.Ile406=) c.999A= (n.999A=) n.881A= c.1303A= (p.Ile435=) c.1315A= (p.Ile439=) | |
| 1 | g.114677919A>C | CA419883080 | AMPD1 | c.1203T>G (p.Thr401=) c.1215T>G (p.Thr405=) c.998T>G (n.998T>G) n.880T>G c.1302T>G (p.Thr434=) c.1314T>G (p.Thr438=) | |
| 1 | g.114677919A>G | CA419883081 | AMPD1 | c.1203T>C (p.Thr401=) c.1215T>C (p.Thr405=) c.998T>C (n.998T>C) n.880T>C c.1302T>C (p.Thr434=) c.1314T>C (p.Thr438=) | |
| 1 | g.114677919A>T | CA419883082 | AMPD1 | c.1203T>A (p.Thr401=) c.1215T>A (p.Thr405=) c.998T>A (n.998T>A) n.880T>A c.1302T>A (p.Thr434=) c.1314T>A (p.Thr438=) | |
| 1 | g.114677920G>A | CA1020190 | AMPD1 | c.1202C>T (p.Thr401Ile) c.1214C>T (p.Thr405Ile) c.997C>T (n.997C>T) n.879C>T c.1301C>T (p.Thr434Ile) c.1313C>T (p.Thr438Ile) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.114677920G>C | CA341748962 | AMPD1 | c.1202C>G (p.Thr401Ser) c.1214C>G (p.Thr405Ser) c.997C>G (n.997C>G) n.879C>G c.1301C>G (p.Thr434Ser) c.1313C>G (p.Thr438Ser) | |
| 1 | g.114677920G= | CA1190276594 | AMPD1 | c.1202C= (p.Thr401=) c.1214C= (p.Thr405=) c.997C= (n.997C=) n.879C= c.1301C= (p.Thr434=) c.1313C= (p.Thr438=) | |
| 1 | g.114677920G>T | CA341748963 | AMPD1 | c.1202C>A (p.Thr401Asn) c.1214C>A (p.Thr405Asn) c.997C>A (n.997C>A) n.879C>A c.1301C>A (p.Thr434Asn) c.1313C>A (p.Thr438Asn) | |
| 1 | g.114677921T>A | CA341748964 | AMPD1 | c.1201A>T (p.Thr401Ser) c.1213A>T (p.Thr405Ser) c.996A>T (n.996A>T) n.878A>T c.1300A>T (p.Thr434Ser) c.1312A>T (p.Thr438Ser) | gnomAD v4 |
| 1 | g.114677921T>C | CA341748965 | AMPD1 | c.1201A>G (p.Thr401Ala) c.1213A>G (p.Thr405Ala) c.996A>G (n.996A>G) n.878A>G c.1300A>G (p.Thr434Ala) c.1312A>G (p.Thr438Ala) | COSMIC COSMIC |
| 1 | g.114677921T>G | CA341748966 | AMPD1 | c.1201A>C (p.Thr401Pro) c.1213A>C (p.Thr405Pro) c.996A>C (n.996A>C) n.878A>C c.1300A>C (p.Thr434Pro) c.1312A>C (p.Thr438Pro) | |
| 1 | g.114677922G>A | CA1020191 | AMPD1 | c.1200C>T (p.Ala400=) c.1212C>T (p.Ala404=) c.995C>T (n.995C>T) n.877C>T c.1299C>T (p.Ala433=) c.1311C>T (p.Ala437=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.114677922G>C | CA419883084 | AMPD1 | c.1200C>G (p.Ala400=) c.1212C>G (p.Ala404=) c.995C>G (n.995C>G) n.877C>G c.1299C>G (p.Ala433=) c.1311C>G (p.Ala437=) | |
| 1 | g.114677922G= | CA1190276595 | AMPD1 | c.1200C= (p.Ala400=) c.1212C= (p.Ala404=) c.995C= (n.995C=) n.877C= c.1299C= (p.Ala433=) c.1311C= (p.Ala437=) | |
| 1 | g.114677922G>T | CA419883083 | AMPD1 | c.1200C>A (p.Ala400=) c.1212C>A (p.Ala404=) c.995C>A (n.995C>A) n.877C>A c.1299C>A (p.Ala433=) c.1311C>A (p.Ala437=) | |
| 1 | g.114677923G>A | CA341748967 | AMPD1 | c.1199C>T (p.Ala400Val) c.1211C>T (p.Ala404Val) c.994C>T (n.994C>T) n.876C>T c.1298C>T (p.Ala433Val) c.1310C>T (p.Ala437Val) | |
| 1 | g.114677923G>C | CA341748968 | AMPD1 | c.1199C>G (p.Ala400Gly) c.1211C>G (p.Ala404Gly) c.994C>G (n.994C>G) n.876C>G c.1298C>G (p.Ala433Gly) c.1310C>G (p.Ala437Gly) | gnomAD v4 |
| 1 | g.114677923G>T | CA341748969 | AMPD1 | c.1199C>A (p.Ala400Asp) c.1211C>A (p.Ala404Asp) c.994C>A (n.994C>A) n.876C>A c.1298C>A (p.Ala433Asp) c.1310C>A (p.Ala437Asp) | |
| 1 | g.114677924C>A | CA341748971 | AMPD1 | c.1198G>T (p.Ala400Ser) c.1210G>T (p.Ala404Ser) c.993G>T (n.993G>T) n.875G>T c.1297G>T (p.Ala433Ser) c.1309G>T (p.Ala437Ser) | |
| 1 | g.114677924C= | CA1190276596 | AMPD1 | c.1198G= (p.Ala400=) c.1210G= (p.Ala404=) c.993G= (n.993G=) n.875G= c.1297G= (p.Ala433=) c.1309G= (p.Ala437=) | |
| 1 | g.114677924C>G | CA341748970 | AMPD1 | c.1198G>C (p.Ala400Pro) c.1210G>C (p.Ala404Pro) c.993G>C (n.993G>C) n.875G>C c.1297G>C (p.Ala433Pro) c.1309G>C (p.Ala437Pro) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.114677924C>T | CA1020192 | AMPD1 | c.1198G>A (p.Ala400Thr) c.1210G>A (p.Ala404Thr) c.993G>A (n.993G>A) n.875G>A c.1297G>A (p.Ala433Thr) c.1309G>A (p.Ala437Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.114677925A= | CA1190276597 | AMPD1 | c.1197T= (p.Phe399=) c.1209T= (p.Phe403=) c.992T= (n.992T=) n.874T= c.1296T= (p.Phe432=) c.1308T= (p.Phe436=) | |
| 1 | g.114677925A>C | CA341748972 | AMPD1 | c.1197T>G (p.Phe399Leu) c.1209T>G (p.Phe403Leu) c.992T>G (n.992T>G) n.874T>G c.1296T>G (p.Phe432Leu) c.1308T>G (p.Phe436Leu) | |
| 1 | g.114677925A>G | CA419883085 | AMPD1 | c.1197T>C (p.Phe399=) c.1209T>C (p.Phe403=) c.992T>C (n.992T>C) n.874T>C c.1296T>C (p.Phe432=) c.1308T>C (p.Phe436=) | dbSNP gnomAD v2 |
| 1 | g.114677925A>T | CA341748973 | AMPD1 | c.1197T>A (p.Phe399Leu) c.1209T>A (p.Phe403Leu) c.992T>A (n.992T>A) n.874T>A c.1296T>A (p.Phe432Leu) c.1308T>A (p.Phe436Leu) | |
| 1 | g.114677926A>C | CA341748974 | AMPD1 | c.1196T>G (p.Phe399Cys) c.1208T>G (p.Phe403Cys) c.991T>G (n.991T>G) n.873T>G c.1295T>G (p.Phe432Cys) c.1307T>G (p.Phe436Cys) | |
| 1 | g.114677926A>G | CA341748975 | AMPD1 | c.1196T>C (p.Phe399Ser) c.1208T>C (p.Phe403Ser) c.991T>C (n.991T>C) n.873T>C c.1295T>C (p.Phe432Ser) c.1307T>C (p.Phe436Ser) | |
| 1 | g.114677926A>T | CA341748976 | AMPD1 | c.1196T>A (p.Phe399Tyr) c.1208T>A (p.Phe403Tyr) c.991T>A (n.991T>A) n.873T>A c.1295T>A (p.Phe432Tyr) c.1307T>A (p.Phe436Tyr) | |
| 1 | g.114677927A= | CA1190276598 | AMPD1 | c.1195T= (p.Phe399=) c.1207T= (p.Phe403=) c.990T= (n.990T=) n.872T= c.1294T= (p.Phe432=) c.1306T= (p.Phe436=) | |
| 1 | g.114677927A>C | CA1020193 | AMPD1 | c.1195T>G (p.Phe399Val) c.1207T>G (p.Phe403Val) c.990T>G (n.990T>G) n.872T>G c.1294T>G (p.Phe432Val) c.1306T>G (p.Phe436Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.114677927A>G | CA341748977 | AMPD1 | c.1195T>C (p.Phe399Leu) c.1207T>C (p.Phe403Leu) c.990T>C (n.990T>C) n.872T>C c.1294T>C (p.Phe432Leu) c.1306T>C (p.Phe436Leu) | |
| 1 | g.114677927A>T | CA341748978 | AMPD1 | c.1195T>A (p.Phe399Ile) c.1207T>A (p.Phe403Ile) c.990T>A (n.990T>A) n.872T>A c.1294T>A (p.Phe432Ile) c.1306T>A (p.Phe436Ile) | |
| 1 | g.114677928A= | CA1190276599 | AMPD1 | c.1194T= (p.Tyr398=) c.1206T= (p.Tyr402=) c.989T= (n.989T=) n.871T= c.1293T= (p.Tyr431=) c.1305T= (p.Tyr435=) | |
| 1 | g.114677928A>C | CA341748979 | AMPD1 | c.1194T>G (p.Tyr398Ter) c.1206T>G (p.Tyr402Ter) c.989T>G (n.989T>G) n.871T>G c.1293T>G (p.Tyr431Ter) c.1305T>G (p.Tyr435Ter) | |
| 1 | g.114677928A>G | CA1020194 | AMPD1 | c.1194T>C (p.Tyr398=) c.1206T>C (p.Tyr402=) c.989T>C (n.989T>C) n.871T>C c.1293T>C (p.Tyr431=) c.1305T>C (p.Tyr435=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 1 | g.114677928A>T | CA341748980 | AMPD1 | c.1194T>A (p.Tyr398Ter) c.1206T>A (p.Tyr402Ter) c.989T>A (n.989T>A) n.871T>A c.1293T>A (p.Tyr431Ter) c.1305T>A (p.Tyr435Ter) | |
| 1 | g.114677929T>A | CA341748981 | AMPD1 | c.1193A>T (p.Tyr398Phe) c.1205A>T (p.Tyr402Phe) c.988A>T (n.988A>T) n.870A>T c.1292A>T (p.Tyr431Phe) c.1304A>T (p.Tyr435Phe) | |
| 1 | g.114677929T>C | CA341748982 | AMPD1 | c.1193A>G (p.Tyr398Cys) c.1205A>G (p.Tyr402Cys) c.988A>G (n.988A>G) n.870A>G c.1292A>G (p.Tyr431Cys) c.1304A>G (p.Tyr435Cys) | |
| 1 | g.114677929T>G | CA341748984 | AMPD1 | c.1193A>C (p.Tyr398Ser) c.1205A>C (p.Tyr402Ser) c.988A>C (n.988A>C) n.870A>C c.1292A>C (p.Tyr431Ser) c.1304A>C (p.Tyr435Ser) | |
| 1 | g.114677930A>C | CA341748987 | AMPD1 | c.1192T>G (p.Tyr398Asp) c.1204T>G (p.Tyr402Asp) c.987T>G (n.987T>G) n.869T>G c.1291T>G (p.Tyr431Asp) c.1303T>G (p.Tyr435Asp) | |
| 1 | g.114677930A>G | CA341748986 | AMPD1 | c.1192T>C (p.Tyr398His) c.1204T>C (p.Tyr402His) c.987T>C (n.987T>C) n.869T>C c.1291T>C (p.Tyr431His) c.1303T>C (p.Tyr435His) | |
| 1 | g.114677930A>T | CA341748985 | AMPD1 | c.1192T>A (p.Tyr398Asn) c.1204T>A (p.Tyr402Asn) c.987T>A (n.987T>A) n.869T>A c.1291T>A (p.Tyr431Asn) c.1303T>A (p.Tyr435Asn) |