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 |
|---|---|---|---|---|---|
| X | g.77870885G>A | CA128812 | MAGT1 | c.313C>T (p.Arg105Ter) n.340C>T c.211C>T (p.Arg71Ter) c.409C>T (p.Arg137Ter) n.327C>T | ClinVar dbSNP COSMIC COSMIC |
| X | g.77870885G>C | CA413711273 | MAGT1 | c.313C>G (p.Arg105Gly) n.340C>G c.211C>G (p.Arg71Gly) c.409C>G (p.Arg137Gly) n.327C>G | |
| X | g.77870885G= | CA2439054259 | MAGT1 | c.313C= (p.Arg105=) n.340C= c.211C= (p.Arg71=) c.409C= (p.Arg137=) n.327C= | |
| X | g.77870885G>T | CA517376539 | MAGT1 | c.313C>A (p.Arg105=) n.340C>A c.211C>A (p.Arg71=) c.409C>A (p.Arg137=) n.327C>A | |
| X | g.77870886C>A | CA413711277 | MAGT1 | c.312G>T (p.Trp104Cys) n.339G>T c.210G>T (p.Trp70Cys) c.408G>T (p.Trp136Cys) n.326G>T | |
| X | g.77870886C>G | CA413711278 | MAGT1 | c.312G>C (p.Trp104Cys) n.339G>C c.210G>C (p.Trp70Cys) c.408G>C (p.Trp136Cys) n.326G>C | |
| X | g.77870886C>T | CA413711280 | MAGT1 | c.312G>A (p.Trp104Ter) n.339G>A c.210G>A (p.Trp70Ter) c.408G>A (p.Trp136Ter) n.326G>A | |
| X | g.77870887C>A | CA413711282 | MAGT1 | c.311G>T (p.Trp104Leu) n.338G>T c.209G>T (p.Trp70Leu) c.407G>T (p.Trp136Leu) n.325G>T | |
| X | g.77870887C>G | CA413711284 | MAGT1 | c.311G>C (p.Trp104Ser) n.338G>C c.209G>C (p.Trp70Ser) c.407G>C (p.Trp136Ser) n.325G>C | |
| X | g.77870887C>T | CA413711285 | MAGT1 | c.311G>A (p.Trp104Ter) n.338G>A c.209G>A (p.Trp70Ter) c.407G>A (p.Trp136Ter) n.325G>A | gnomAD v4 |
| X | g.77870888A>C | CA413711290 | MAGT1 | c.310T>G (p.Trp104Gly) n.337T>G c.208T>G (p.Trp70Gly) c.406T>G (p.Trp136Gly) n.324T>G | |
| X | g.77870888A>G | CA413711287 | MAGT1 | c.310T>C (p.Trp104Arg) n.337T>C c.208T>C (p.Trp70Arg) c.406T>C (p.Trp136Arg) n.324T>C | |
| X | g.77870888A>T | CA413711288 | MAGT1 | c.310T>A (p.Trp104Arg) n.337T>A c.208T>A (p.Trp70Arg) c.406T>A (p.Trp136Arg) n.324T>A | |
| X | g.77870889G>A | CA10458560 | MAGT1 | c.309C>T (p.Ser103=) n.336C>T c.207C>T (p.Ser69=) c.405C>T (p.Ser135=) n.323C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.77870889G>C | CA517376541 | MAGT1 | c.309C>G (p.Ser103=) n.336C>G c.207C>G (p.Ser69=) c.405C>G (p.Ser135=) n.323C>G | |
| X | g.77870889G= | CA2439054260 | MAGT1 | c.309C= (p.Ser103=) n.336C= c.207C= (p.Ser69=) c.405C= (p.Ser135=) n.323C= | |
| X | g.77870889G>T | CA517376540 | MAGT1 | c.309C>A (p.Ser103=) n.336C>A c.207C>A (p.Ser69=) c.405C>A (p.Ser135=) n.323C>A | |
| X | g.77870890G>A | CA413711291 | MAGT1 | c.308C>T (p.Ser103Phe) n.335C>T c.206C>T (p.Ser69Phe) c.404C>T (p.Ser135Phe) n.322C>T | |
| X | g.77870890G>C | CA413711292 | MAGT1 | c.308C>G (p.Ser103Cys) n.335C>G c.206C>G (p.Ser69Cys) c.404C>G (p.Ser135Cys) n.322C>G | |
| X | g.77870890G>T | CA413711293 | MAGT1 | c.308C>A (p.Ser103Tyr) n.335C>A c.206C>A (p.Ser69Tyr) c.404C>A (p.Ser135Tyr) n.322C>A | |
| X | g.77870891A>C | CA413711295 | MAGT1 | c.307T>G (p.Ser103Ala) n.334T>G c.205T>G (p.Ser69Ala) c.403T>G (p.Ser135Ala) n.321T>G | |
| X | g.77870891A>G | CA413711297 | MAGT1 | c.307T>C (p.Ser103Pro) n.334T>C c.205T>C (p.Ser69Pro) c.403T>C (p.Ser135Pro) n.321T>C | |
| X | g.77870891A>T | CA413711299 | MAGT1 | c.307T>A (p.Ser103Thr) n.334T>A c.205T>A (p.Ser69Thr) c.403T>A (p.Ser135Thr) n.321T>A | |
| X | g.77870892G>A | CA517376543 | MAGT1 | c.306C>T (p.Asn102=) n.333C>T c.204C>T (p.Asn68=) c.402C>T (p.Asn134=) n.320C>T | |
| X | g.77870892G>C | CA413711300 | MAGT1 | c.306C>G (p.Asn102Lys) n.333C>G c.204C>G (p.Asn68Lys) c.402C>G (p.Asn134Lys) n.320C>G | |
| X | g.77870892G>T | CA413711301 | MAGT1 | c.306C>A (p.Asn102Lys) n.333C>A c.204C>A (p.Asn68Lys) c.402C>A (p.Asn134Lys) n.320C>A | |
| X | g.77870893T>A | CA413711303 | MAGT1 | c.305A>T (p.Asn102Ile) n.332A>T c.203A>T (p.Asn68Ile) c.401A>T (p.Asn134Ile) n.319A>T | |
| X | g.77870893T>C | CA413711304 | MAGT1 | c.305A>G (p.Asn102Ser) n.332A>G c.203A>G (p.Asn68Ser) c.401A>G (p.Asn134Ser) n.319A>G | |
| X | g.77870893T>G | CA413711305 | MAGT1 | c.305A>C (p.Asn102Thr) n.332A>C c.203A>C (p.Asn68Thr) c.401A>C (p.Asn134Thr) n.319A>C | |
| X | g.77870894T>A | CA413711308 | MAGT1 | c.304A>T (p.Asn102Tyr) n.331A>T c.202A>T (p.Asn68Tyr) c.400A>T (p.Asn134Tyr) n.318A>T | |
| X | g.77870894T>C | CA413711306 | MAGT1 | c.304A>G (p.Asn102Asp) n.331A>G c.202A>G (p.Asn68Asp) c.400A>G (p.Asn134Asp) n.318A>G | |
| X | g.77870894T>G | CA413711307 | MAGT1 | c.304A>C (p.Asn102His) n.331A>C c.202A>C (p.Asn68His) c.400A>C (p.Asn134His) n.318A>C | |
| X | g.77870895T>A | CA517376544 | MAGT1 | c.303A>T (p.Ala101=) n.330A>T c.201A>T (p.Ala67=) c.399A>T (p.Ala133=) n.317A>T | |
| X | g.77870895T>C | CA517376545 | MAGT1 | c.303A>G (p.Ala101=) n.330A>G c.201A>G (p.Ala67=) c.399A>G (p.Ala133=) n.317A>G | |
| X | g.77870895T>G | CA517376546 | MAGT1 | c.303A>C (p.Ala101=) n.330A>C c.201A>C (p.Ala67=) c.399A>C (p.Ala133=) n.317A>C | |
| X | g.77870896G>A | CA413711309 | MAGT1 | c.302C>T (p.Ala101Val) n.329C>T c.200C>T (p.Ala67Val) c.398C>T (p.Ala133Val) n.316C>T | |
| X | g.77870896G>C | CA413711310 | MAGT1 | c.302C>G (p.Ala101Gly) n.329C>G c.200C>G (p.Ala67Gly) c.398C>G (p.Ala133Gly) n.316C>G | |
| X | g.77870896G>T | CA413711312 | MAGT1 | c.302C>A (p.Ala101Glu) n.329C>A c.200C>A (p.Ala67Glu) c.398C>A (p.Ala133Glu) n.316C>A | |
| X | g.77870897C>A | CA413711313 | MAGT1 | c.301G>T (p.Ala101Ser) n.328G>T c.199G>T (p.Ala67Ser) c.397G>T (p.Ala133Ser) n.315G>T | |
| X | g.77870897C= | CA2439054261 | MAGT1 | c.301G= (p.Ala101=) n.328G= c.199G= (p.Ala67=) c.397G= (p.Ala133=) n.315G= | |
| X | g.77870897C>G | CA413711314 | MAGT1 | c.301G>C (p.Ala101Pro) n.328G>C c.199G>C (p.Ala67Pro) c.397G>C (p.Ala133Pro) n.315G>C | |
| X | g.77870897C>T | CA413711316 | MAGT1 | c.301G>A (p.Ala101Thr) n.328G>A c.199G>A (p.Ala67Thr) c.397G>A (p.Ala133Thr) n.315G>A | dbSNP gnomAD v4 |
| X | g.77870898C>A | CA517376548 | MAGT1 | c.300G>T (p.Leu100=) n.327G>T c.198G>T (p.Leu66=) c.396G>T (p.Leu132=) n.314G>T | |
| X | g.77870898C= | CA2439054262 | MAGT1 | c.300G= (p.Leu100=) n.327G= c.198G= (p.Leu66=) c.396G= (p.Leu132=) n.314G= | |
| X | g.77870898C>G | CA517376549 | MAGT1 | c.300G>C (p.Leu100=) n.327G>C c.198G>C (p.Leu66=) c.396G>C (p.Leu132=) n.314G>C | |
| X | g.77870898C>T | CA517376550 | MAGT1 | c.300G>A (p.Leu100=) n.327G>A c.198G>A (p.Leu66=) c.396G>A (p.Leu132=) n.314G>A | dbSNP gnomAD v2 gnomAD v4 |
| X | g.77870899A>C | CA413711320 | MAGT1 | c.299T>G (p.Leu100Arg) n.326T>G c.197T>G (p.Leu66Arg) c.395T>G (p.Leu132Arg) n.313T>G | |
| X | g.77870899A>G | CA413711318 | MAGT1 | c.299T>C (p.Leu100Pro) n.326T>C c.197T>C (p.Leu66Pro) c.395T>C (p.Leu132Pro) n.313T>C | |
| X | g.77870899A>T | CA413711317 | MAGT1 | c.299T>A (p.Leu100Gln) n.326T>A c.197T>A (p.Leu66Gln) c.395T>A (p.Leu132Gln) n.313T>A | |
| X | g.77870900G>A | CA517376552 | MAGT1 | c.298C>T (p.Leu100=) n.325C>T c.196C>T (p.Leu66=) c.394C>T (p.Leu132=) n.312C>T |