WARNING - Protein Allele ID and Protein Sequence HGVS API Requests Temporarily Disabled:
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 6 | g.29672650A= | CA1618398830 | ZFP57 | c.1461T= (p.His487=) c.1245T= (p.His415=) c.1209T= (p.His403=) c.1401T= (p.His467=) | |
| 6 | g.29672650A>C | CA363043127 | ZFP57 | c.1461T>G (p.His487Gln) c.1245T>G (p.His415Gln) c.1209T>G (p.His403Gln) c.1401T>G (p.His467Gln) | gnomAD v4 |
| 6 | g.29672650A>G | CA449458329 | ZFP57 | c.1461T>C (p.His487=) c.1245T>C (p.His415=) c.1209T>C (p.His403=) c.1401T>C (p.His467=) | |
| 6 | g.29672650A>T | CA363043128 | ZFP57 | c.1461T>A (p.His487Gln) c.1245T>A (p.His415Gln) c.1209T>A (p.His403Gln) c.1401T>A (p.His467Gln) | dbSNP gnomAD v2 gnomAD v4 |
| 6 | g.29672651T>A | CA363043129 | ZFP57 | c.1460A>T (p.His487Leu) c.1244A>T (p.His415Leu) c.1208A>T (p.His403Leu) c.1400A>T (p.His467Leu) | gnomAD v4 |
| 6 | g.29672651T>C | CA363043130 | ZFP57 | c.1460A>G (p.His487Arg) c.1244A>G (p.His415Arg) c.1208A>G (p.His403Arg) c.1400A>G (p.His467Arg) | dbSNP gnomAD v4 |
| 6 | g.29672651T>G | CA363043132 | ZFP57 | c.1460A>C (p.His487Pro) c.1244A>C (p.His415Pro) c.1208A>C (p.His403Pro) c.1400A>C (p.His467Pro) | |
| 6 | g.29672651T= | CA1618398831 | ZFP57 | c.1460A= (p.His487=) c.1244A= (p.His415=) c.1208A= (p.His403=) c.1400A= (p.His467=) | |
| 6 | g.29672652G>A | CA3690680 | ZFP57 | c.1459C>T (p.His487Tyr) c.1243C>T (p.His415Tyr) c.1207C>T (p.His403Tyr) c.1399C>T (p.His467Tyr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 6 | g.29672652G>C | CA363043133 | ZFP57 | c.1459C>G (p.His487Asp) c.1243C>G (p.His415Asp) c.1207C>G (p.His403Asp) c.1399C>G (p.His467Asp) | |
| 6 | g.29672652G= | CA1618398832 | ZFP57 | c.1459C= (p.His487=) c.1243C= (p.His415=) c.1207C= (p.His403=) c.1399C= (p.His467=) | |
| 6 | g.29672652G>T | CA363043134 | ZFP57 | c.1459C>A (p.His487Asn) c.1243C>A (p.His415Asn) c.1207C>A (p.His403Asn) c.1399C>A (p.His467Asn) | |
| 6 | g.29672653A>C | CA449458223 | ZFP57 | c.1458T>G (p.Ser486=) c.1242T>G (p.Ser414=) c.1206T>G (p.Ser402=) c.1398T>G (p.Ser466=) | |
| 6 | g.29672653A>G | CA449458224 | ZFP57 | c.1458T>C (p.Ser486=) c.1242T>C (p.Ser414=) c.1206T>C (p.Ser402=) c.1398T>C (p.Ser466=) | |
| 6 | g.29672653A>T | CA449458225 | ZFP57 | c.1458T>A (p.Ser486=) c.1242T>A (p.Ser414=) c.1206T>A (p.Ser402=) c.1398T>A (p.Ser466=) | |
| 6 | g.29672654G>A | CA363043135 | ZFP57 | c.1457C>T (p.Ser486Phe) c.1241C>T (p.Ser414Phe) c.1205C>T (p.Ser402Phe) c.1397C>T (p.Ser466Phe) | dbSNP gnomAD v4 |
| 6 | g.29672654G>C | CA363043137 | ZFP57 | c.1457C>G (p.Ser486Cys) c.1241C>G (p.Ser414Cys) c.1205C>G (p.Ser402Cys) c.1397C>G (p.Ser466Cys) | |
| 6 | g.29672654G= | CA1618398833 | ZFP57 | c.1457C= (p.Ser486=) c.1241C= (p.Ser414=) c.1205C= (p.Ser402=) c.1397C= (p.Ser466=) | |
| 6 | g.29672654G>T | CA363043139 | ZFP57 | c.1457C>A (p.Ser486Tyr) c.1241C>A (p.Ser414Tyr) c.1205C>A (p.Ser402Tyr) c.1397C>A (p.Ser466Tyr) | |
| 6 | g.29672655A>C | CA363043140 | ZFP57 | c.1456T>G (p.Ser486Ala) c.1240T>G (p.Ser414Ala) c.1204T>G (p.Ser402Ala) c.1396T>G (p.Ser466Ala) | |
| 6 | g.29672655A>G | CA363043141 | ZFP57 | c.1456T>C (p.Ser486Pro) c.1240T>C (p.Ser414Pro) c.1204T>C (p.Ser402Pro) c.1396T>C (p.Ser466Pro) | |
| 6 | g.29672655A>T | CA363043143 | ZFP57 | c.1456T>A (p.Ser486Thr) c.1240T>A (p.Ser414Thr) c.1204T>A (p.Ser402Thr) c.1396T>A (p.Ser466Thr) | |
| 6 | g.29672656G>A | CA449458229 | ZFP57 | c.1455C>T (p.Phe485=) c.1239C>T (p.Phe413=) c.1203C>T (p.Phe401=) c.1395C>T (p.Phe465=) | dbSNP gnomAD v2 gnomAD v4 |
| 6 | g.29672656G>C | CA363043145 | ZFP57 | c.1455C>G (p.Phe485Leu) c.1239C>G (p.Phe413Leu) c.1203C>G (p.Phe401Leu) c.1395C>G (p.Phe465Leu) | |
| 6 | g.29672656G= | CA1618398834 | ZFP57 | c.1455C= (p.Phe485=) c.1239C= (p.Phe413=) c.1203C= (p.Phe401=) c.1395C= (p.Phe465=) | |
| 6 | g.29672656G>T | CA363043147 | ZFP57 | c.1455C>A (p.Phe485Leu) c.1239C>A (p.Phe413Leu) c.1203C>A (p.Phe401Leu) c.1395C>A (p.Phe465Leu) | dbSNP gnomAD v2 gnomAD v4 |
| 6 | g.29672657A>C | CA363043148 | ZFP57 | c.1454T>G (p.Phe485Cys) c.1238T>G (p.Phe413Cys) c.1202T>G (p.Phe401Cys) c.1394T>G (p.Phe465Cys) | |
| 6 | g.29672657A>G | CA363043149 | ZFP57 | c.1454T>C (p.Phe485Ser) c.1238T>C (p.Phe413Ser) c.1202T>C (p.Phe401Ser) c.1394T>C (p.Phe465Ser) | |
| 6 | g.29672657A>T | CA363043150 | ZFP57 | c.1454T>A (p.Phe485Tyr) c.1238T>A (p.Phe413Tyr) c.1202T>A (p.Phe401Tyr) c.1394T>A (p.Phe465Tyr) | |
| 6 | g.29672658A>C | CA363043153 | ZFP57 | c.1453T>G (p.Phe485Val) c.1237T>G (p.Phe413Val) c.1201T>G (p.Phe401Val) c.1393T>G (p.Phe465Val) | gnomAD v4 |
| 6 | g.29672658A>G | CA363043152 | ZFP57 | c.1453T>C (p.Phe485Leu) c.1237T>C (p.Phe413Leu) c.1201T>C (p.Phe401Leu) c.1393T>C (p.Phe465Leu) | |
| 6 | g.29672658A>T | CA363043151 | ZFP57 | c.1453T>A (p.Phe485Ile) c.1237T>A (p.Phe413Ile) c.1201T>A (p.Phe401Ile) c.1393T>A (p.Phe465Ile) | |
| 6 | g.29672659G>A | CA449458241 | ZFP57 | c.1452C>T (p.Gly484=) c.1236C>T (p.Gly412=) c.1200C>T (p.Gly400=) c.1392C>T (p.Gly464=) | |
| 6 | g.29672659G>C | CA449458240 | ZFP57 | c.1452C>G (p.Gly484=) c.1236C>G (p.Gly412=) c.1200C>G (p.Gly400=) c.1392C>G (p.Gly464=) | |
| 6 | g.29672659G= | CA1618398835 | ZFP57 | c.1452C= (p.Gly484=) c.1236C= (p.Gly412=) c.1200C= (p.Gly400=) c.1392C= (p.Gly464=) | |
| 6 | g.29672659G>T | CA135974382 | ZFP57 | c.1452C>A (p.Gly484=) c.1236C>A (p.Gly412=) c.1200C>A (p.Gly400=) c.1392C>A (p.Gly464=) | dbSNP |
| 6 | g.29672660C>A | CA363043154 | ZFP57 | c.1451G>T (p.Gly484Val) c.1235G>T (p.Gly412Val) c.1199G>T (p.Gly400Val) c.1391G>T (p.Gly464Val) | gnomAD v4 |
| 6 | g.29672660C= | CA1618398836 | ZFP57 | c.1451G= (p.Gly484=) c.1235G= (p.Gly412=) c.1199G= (p.Gly400=) c.1391G= (p.Gly464=) | |
| 6 | g.29672660C>G | CA363043155 | ZFP57 | c.1451G>C (p.Gly484Ala) c.1235G>C (p.Gly412Ala) c.1199G>C (p.Gly400Ala) c.1391G>C (p.Gly464Ala) | dbSNP |
| 6 | g.29672660C>T | CA363043156 | ZFP57 | c.1451G>A (p.Gly484Asp) c.1235G>A (p.Gly412Asp) c.1199G>A (p.Gly400Asp) c.1391G>A (p.Gly464Asp) | |
| 6 | g.29672661C>A | CA363043157 | ZFP57 | c.1450G>T (p.Gly484Cys) c.1234G>T (p.Gly412Cys) c.1198G>T (p.Gly400Cys) c.1390G>T (p.Gly464Cys) | gnomAD v4 |
| 6 | g.29672661C= | CA1618398837 | ZFP57 | c.1450G= (p.Gly484=) c.1234G= (p.Gly412=) c.1198G= (p.Gly400=) c.1390G= (p.Gly464=) | |
| 6 | g.29672661C>G | CA363043158 | ZFP57 | c.1450G>C (p.Gly484Arg) c.1234G>C (p.Gly412Arg) c.1198G>C (p.Gly400Arg) c.1390G>C (p.Gly464Arg) | |
| 6 | g.29672661C>T | CA363043159 | ZFP57 | c.1450G>A (p.Gly484Ser) c.1234G>A (p.Gly412Ser) c.1198G>A (p.Gly400Ser) c.1390G>A (p.Gly464Ser) | dbSNP gnomAD v2 gnomAD v4 |
| 6 | g.29672662A>C | CA449458242 | ZFP57 | c.1449T>G (p.Leu483=) c.1233T>G (p.Leu411=) c.1197T>G (p.Leu399=) c.1389T>G (p.Leu463=) | |
| 6 | g.29672662A>G | CA449458243 | ZFP57 | c.1449T>C (p.Leu483=) c.1233T>C (p.Leu411=) c.1197T>C (p.Leu399=) c.1389T>C (p.Leu463=) | |
| 6 | g.29672662A>T | CA449458244 | ZFP57 | c.1449T>A (p.Leu483=) c.1233T>A (p.Leu411=) c.1197T>A (p.Leu399=) c.1389T>A (p.Leu463=) | |
| 6 | g.29672663A>C | CA363043160 | ZFP57 | c.1448T>G (p.Leu483Arg) c.1232T>G (p.Leu411Arg) c.1196T>G (p.Leu399Arg) c.1388T>G (p.Leu463Arg) | COSMIC |
| 6 | g.29672663A>G | CA363043161 | ZFP57 | c.1448T>C (p.Leu483Pro) c.1232T>C (p.Leu411Pro) c.1196T>C (p.Leu399Pro) c.1388T>C (p.Leu463Pro) | |
| 6 | g.29672663A>T | CA363043162 | ZFP57 | c.1448T>A (p.Leu483His) c.1232T>A (p.Leu411His) c.1196T>A (p.Leu399His) c.1388T>A (p.Leu463His) | COSMIC |