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 |
|---|---|---|---|---|---|
| 1 | g.161673970T>A | CA421420347 | FCGR2B | c.657T>A (p.Ser219=) c.636T>A (p.Ser212=) n.707T>A n.2025T>A c.654T>A (p.Ser218=) c.633T>A (p.Ser211=) n.886T>A | |
| 1 | g.161673970T>C | CA421420348 | FCGR2B | c.657T>C (p.Ser219=) c.636T>C (p.Ser212=) n.707T>C n.2025T>C c.654T>C (p.Ser218=) c.633T>C (p.Ser211=) n.886T>C | |
| 1 | g.161673970T>G | CA421420351 | FCGR2B | c.657T>G (p.Ser219=) c.636T>G (p.Ser212=) n.707T>G n.2025T>G c.654T>G (p.Ser218=) c.633T>G (p.Ser211=) n.886T>G | dbSNP |
| 1 | g.161673970T= | CA1202839739 | FCGR2B | c.657T= (p.Ser219=) c.636T= (p.Ser212=) n.707T= n.2025T= c.654T= (p.Ser218=) c.633T= (p.Ser211=) n.886T= | |
| 1 | g.161673971T>A | CA343367482 | FCGR2B | c.658T>A (p.Ser220Thr) c.637T>A (p.Ser213Thr) n.708T>A n.2026T>A c.655T>A (p.Ser219Thr) c.634T>A (p.Ser212Thr) n.887T>A | |
| 1 | g.161673971T>C | CA343367484 | FCGR2B | c.658T>C (p.Ser220Pro) c.637T>C (p.Ser213Pro) n.708T>C n.2026T>C c.655T>C (p.Ser219Pro) c.634T>C (p.Ser212Pro) n.887T>C | |
| 1 | g.161673971T>G | CA343367487 | FCGR2B | c.658T>G (p.Ser220Ala) c.637T>G (p.Ser213Ala) n.708T>G n.2026T>G c.655T>G (p.Ser219Ala) c.634T>G (p.Ser212Ala) n.887T>G | |
| 1 | g.161673972C>A | CA343367490 | FCGR2B | c.659C>A (p.Ser220Ter) c.638C>A (p.Ser213Ter) n.709C>A n.2027C>A c.656C>A (p.Ser219Ter) c.635C>A (p.Ser212Ter) n.888C>A | |
| 1 | g.161673972C>G | CA343367492 | FCGR2B | c.659C>G (p.Ser220Ter) c.638C>G (p.Ser213Ter) n.709C>G n.2027C>G c.656C>G (p.Ser219Ter) c.635C>G (p.Ser212Ter) n.888C>G | |
| 1 | g.161673972C>T | CA343367495 | FCGR2B | c.659C>T (p.Ser220Leu) c.638C>T (p.Ser213Leu) n.709C>T n.2027C>T c.656C>T (p.Ser219Leu) c.635C>T (p.Ser212Leu) n.888C>T | gnomAD v4 |
| 1 | g.161673973A= | CA1202839740 | FCGR2B | c.660A= (p.Ser220=) c.639A= (p.Ser213=) n.710A= n.2028A= c.657A= (p.Ser219=) c.636A= (p.Ser212=) n.889A= | |
| 1 | g.161673973A>C | CA421420366 | FCGR2B | c.660A>C (p.Ser220=) c.639A>C (p.Ser213=) n.710A>C n.2028A>C c.657A>C (p.Ser219=) c.636A>C (p.Ser212=) n.889A>C | dbSNP |
| 1 | g.161673973A>G | CA421420364 | FCGR2B | c.660A>G (p.Ser220=) c.639A>G (p.Ser213=) n.710A>G n.2028A>G c.657A>G (p.Ser219=) c.636A>G (p.Ser212=) n.889A>G | |
| 1 | g.161673973A>T | CA421420362 | FCGR2B | c.660A>T (p.Ser220=) c.639A>T (p.Ser213=) n.710A>T n.2028A>T c.657A>T (p.Ser219=) c.636A>T (p.Ser212=) n.889A>T | |
| 1 | g.161673974C>A | CA343367497 | FCGR2B | c.661C>A (p.Pro221Thr) c.640C>A (p.Pro214Thr) n.711C>A n.2029C>A c.658C>A (p.Pro220Thr) c.637C>A (p.Pro213Thr) n.890C>A | gnomAD v4 |
| 1 | g.161673974C>G | CA343367499 | FCGR2B | c.661C>G (p.Pro221Ala) c.640C>G (p.Pro214Ala) n.711C>G n.2029C>G c.658C>G (p.Pro220Ala) c.637C>G (p.Pro213Ala) n.890C>G | |
| 1 | g.161673974C>T | CA343367501 | FCGR2B | c.661C>T (p.Pro221Ser) c.640C>T (p.Pro214Ser) n.711C>T n.2029C>T c.658C>T (p.Pro220Ser) c.637C>T (p.Pro213Ser) n.890C>T | |
| 1 | g.161673975C>A | CA343367516 | FCGR2B | c.662C>A (p.Pro221Gln) c.641C>A (p.Pro214Gln) n.712C>A n.2030C>A c.659C>A (p.Pro220Gln) c.638C>A (p.Pro213Gln) n.891C>A | |
| 1 | g.161673975C= | CA1202839741 | FCGR2B | c.662C= (p.Pro221=) c.641C= (p.Pro214=) n.712C= n.2030C= c.659C= (p.Pro220=) c.638C= (p.Pro213=) n.891C= | |
| 1 | g.161673975C>G | CA343367505 | FCGR2B | c.662C>G (p.Pro221Arg) c.641C>G (p.Pro214Arg) n.712C>G n.2030C>G c.659C>G (p.Pro220Arg) c.638C>G (p.Pro213Arg) n.891C>G | |
| 1 | g.161673975C>T | CA343367503 | FCGR2B | c.662C>T (p.Pro221Leu) c.641C>T (p.Pro214Leu) n.712C>T n.2030C>T c.659C>T (p.Pro220Leu) c.638C>T (p.Pro213Leu) n.891C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 1 | g.161673976G>A | CA421420376 | FCGR2B | c.663G>A (p.Pro221=) c.642G>A (p.Pro214=) n.713G>A n.2031G>A c.660G>A (p.Pro220=) c.639G>A (p.Pro213=) n.892G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.161673976G>C | CA421420378 | FCGR2B | c.663G>C (p.Pro221=) c.642G>C (p.Pro214=) n.713G>C n.2031G>C c.660G>C (p.Pro220=) c.639G>C (p.Pro213=) n.892G>C | |
| 1 | g.161673976G= | CA1202839742 | FCGR2B | c.663G= (p.Pro221=) c.642G= (p.Pro214=) n.713G= n.2031G= c.660G= (p.Pro220=) c.639G= (p.Pro213=) n.892G= | |
| 1 | g.161673976G>T | CA421420381 | FCGR2B | c.663G>T (p.Pro221=) c.642G>T (p.Pro214=) n.713G>T n.2031G>T c.660G>T (p.Pro220=) c.639G>T (p.Pro213=) n.892G>T | dbSNP gnomAD v4 |
| 1 | g.161673977A= | CA1202839743 | FCGR2B | c.664A= (p.Met222=) c.643A= (p.Met215=) n.714A= n.2032A= c.661A= (p.Met221=) c.640A= (p.Met214=) n.893A= | |
| 1 | g.161673977A>C | CA343367521 | FCGR2B | c.664A>C (p.Met222Leu) c.643A>C (p.Met215Leu) n.714A>C n.2032A>C c.661A>C (p.Met221Leu) c.640A>C (p.Met214Leu) n.893A>C | |
| 1 | g.161673977A>G | CA343367518 | FCGR2B | c.664A>G (p.Met222Val) c.643A>G (p.Met215Val) n.714A>G n.2032A>G c.661A>G (p.Met221Val) c.640A>G (p.Met214Val) n.893A>G | dbSNP gnomAD v2 gnomAD v4 |
| 1 | g.161673977A>T | CA343367519 | FCGR2B | c.664A>T (p.Met222Leu) c.643A>T (p.Met215Leu) n.714A>T n.2032A>T c.661A>T (p.Met221Leu) c.640A>T (p.Met214Leu) n.893A>T | |
| 1 | g.161673978T>A | CA343367525 | FCGR2B | c.665T>A (p.Met222Lys) c.644T>A (p.Met215Lys) n.715T>A n.2033T>A c.662T>A (p.Met221Lys) c.641T>A (p.Met214Lys) n.894T>A | |
| 1 | g.161673978T>C | CA343367526 | FCGR2B | c.665T>C (p.Met222Thr) c.644T>C (p.Met215Thr) n.715T>C n.2033T>C c.662T>C (p.Met221Thr) c.641T>C (p.Met214Thr) n.894T>C | gnomAD v4 |
| 1 | g.161673978T>G | CA343367527 | FCGR2B | c.665T>G (p.Met222Arg) c.644T>G (p.Met215Arg) n.715T>G n.2033T>G c.662T>G (p.Met221Arg) c.641T>G (p.Met214Arg) n.894T>G | gnomAD v3 gnomAD v4 |
| 1 | g.161673979G>A | CA343367540 | FCGR2B | c.666G>A (p.Met222Ile) c.645G>A (p.Met215Ile) n.716G>A n.2034G>A c.663G>A (p.Met221Ile) c.642G>A (p.Met214Ile) n.895G>A | |
| 1 | g.161673979G>C | CA343367538 | FCGR2B | c.666G>C (p.Met222Ile) c.645G>C (p.Met215Ile) n.716G>C n.2034G>C c.663G>C (p.Met221Ile) c.642G>C (p.Met214Ile) n.895G>C | |
| 1 | g.161673979G>T | CA343367535 | FCGR2B | c.666G>T (p.Met222Ile) c.645G>T (p.Met215Ile) n.716G>T n.2034G>T c.663G>T (p.Met221Ile) c.642G>T (p.Met214Ile) n.895G>T | |
| 1 | g.161673980G>A | CA343367542 | FCGR2B | c.667G>A (p.Gly223Arg) c.646G>A (p.Gly216Arg) n.717G>A n.2035G>A c.664G>A (p.Gly222Arg) c.643G>A (p.Gly215Arg) n.896G>A | dbSNP |
| 1 | g.161673980G>C | CA343367544 | FCGR2B | c.667G>C (p.Gly223Arg) c.646G>C (p.Gly216Arg) n.717G>C n.2035G>C c.664G>C (p.Gly222Arg) c.643G>C (p.Gly215Arg) n.896G>C | |
| 1 | g.161673980G= | CA1202839744 | FCGR2B | c.667G= (p.Gly223=) c.646G= (p.Gly216=) n.717G= n.2035G= c.664G= (p.Gly222=) c.643G= (p.Gly215=) n.896G= | |
| 1 | g.161673980G>T | CA343367546 | FCGR2B | c.667G>T (p.Gly223Trp) c.646G>T (p.Gly216Trp) n.717G>T n.2035G>T c.664G>T (p.Gly222Trp) c.643G>T (p.Gly215Trp) n.896G>T | |
| 1 | g.161673981G>A | CA343367556 | FCGR2B | c.668G>A (p.Gly223Glu) c.647G>A (p.Gly216Glu) n.718G>A n.2036G>A c.665G>A (p.Gly222Glu) c.644G>A (p.Gly215Glu) n.897G>A | |
| 1 | g.161673981G>C | CA343367558 | FCGR2B | c.668G>C (p.Gly223Ala) c.647G>C (p.Gly216Ala) n.718G>C n.2036G>C c.665G>C (p.Gly222Ala) c.644G>C (p.Gly215Ala) n.897G>C | |
| 1 | g.161673981G>T | CA343367560 | FCGR2B | c.668G>T (p.Gly223Val) c.647G>T (p.Gly216Val) n.718G>T n.2036G>T c.665G>T (p.Gly222Val) c.644G>T (p.Gly215Val) n.897G>T | |
| 1 | g.161673982G>A | CA421420399 | FCGR2B | c.669G>A (p.Gly223=) c.648G>A (p.Gly216=) n.719G>A n.2037G>A c.666G>A (p.Gly222=) c.645G>A (p.Gly215=) n.898G>A | |
| 1 | g.161673982G>C | CA421420400 | FCGR2B | c.669G>C (p.Gly223=) c.648G>C (p.Gly216=) n.719G>C n.2037G>C c.666G>C (p.Gly222=) c.645G>C (p.Gly215=) n.898G>C | |
| 1 | g.161673982G= | CA1202839745 | FCGR2B | c.669G= (p.Gly223=) c.648G= (p.Gly216=) n.719G= n.2037G= c.666G= (p.Gly222=) c.645G= (p.Gly215=) n.898G= | |
| 1 | g.161673982G>T | CA421420403 | FCGR2B | c.669G>T (p.Gly223=) c.648G>T (p.Gly216=) n.719G>T n.2037G>T c.666G>T (p.Gly222=) c.645G>T (p.Gly215=) n.898G>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.161673983A= | CA1202839746 | FCGR2B | c.670A= (p.Ile224=) c.649A= (p.Ile217=) n.720A= n.2038A= c.667A= (p.Ile223=) c.646A= (p.Ile216=) n.899A= | |
| 1 | g.161673983A>C | CA343367562 | FCGR2B | c.670A>C (p.Ile224Leu) c.649A>C (p.Ile217Leu) n.720A>C n.2038A>C c.667A>C (p.Ile223Leu) c.646A>C (p.Ile216Leu) n.899A>C | |
| 1 | g.161673983A>G | CA31694570 | FCGR2B | c.670A>G (p.Ile224Val) c.649A>G (p.Ile217Val) n.720A>G n.2038A>G c.667A>G (p.Ile223Val) c.646A>G (p.Ile216Val) n.899A>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 1 | g.161673983A>T | CA343367563 | FCGR2B | c.670A>T (p.Ile224Phe) c.649A>T (p.Ile217Phe) n.720A>T n.2038A>T c.667A>T (p.Ile223Phe) c.646A>T (p.Ile216Phe) n.899A>T | gnomAD v4 |