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 |
|---|---|---|---|---|---|
| 9 | g.91724453C>A | CA373796402 | ROR2 | c.2041G>T (p.Val681Phe) c.1621G>T (p.Val541Phe) n.2509G>T c.838G>T (p.Val280Phe) c.2032G>T (p.Val678Phe) | COSMIC |
| 9 | g.91724453C>G | CA373796403 | ROR2 | c.2041G>C (p.Val681Leu) c.1621G>C (p.Val541Leu) n.2509G>C c.838G>C (p.Val280Leu) c.2032G>C (p.Val678Leu) | gnomAD v4 |
| 9 | g.91724453C>T | CA373796404 | ROR2 | c.2041G>A (p.Val681Ile) c.1621G>A (p.Val541Ile) n.2509G>A c.838G>A (p.Val280Ile) c.2032G>A (p.Val678Ile) | |
| 9 | g.91724454C>A | CA466339052 | ROR2 | c.2040G>T (p.Val680=) c.1620G>T (p.Val540=) n.2508G>T c.837G>T (p.Val279=) c.2031G>T (p.Val677=) | |
| 9 | g.91724454C>G | CA466339056 | ROR2 | c.2040G>C (p.Val680=) c.1620G>C (p.Val540=) n.2508G>C c.837G>C (p.Val279=) c.2031G>C (p.Val677=) | |
| 9 | g.91724454C>T | CA466339054 | ROR2 | c.2040G>A (p.Val680=) c.1620G>A (p.Val540=) n.2508G>A c.837G>A (p.Val279=) c.2031G>A (p.Val677=) | |
| 9 | g.91724455A= | CA1863922793 | ROR2 | c.2039T= (p.Val680=) c.1619T= (p.Val540=) n.2507T= c.836T= (p.Val279=) c.2030T= (p.Val677=) | |
| 9 | g.91724455A>C | CA373796405 | ROR2 | c.2039T>G (p.Val680Gly) c.1619T>G (p.Val540Gly) n.2507T>G c.836T>G (p.Val279Gly) c.2030T>G (p.Val677Gly) | |
| 9 | g.91724455A>G | CA373796409 | ROR2 | c.2039T>C (p.Val680Ala) c.1619T>C (p.Val540Ala) n.2507T>C c.836T>C (p.Val279Ala) c.2030T>C (p.Val677Ala) | dbSNP |
| 9 | g.91724455A>T | CA373796407 | ROR2 | c.2039T>A (p.Val680Glu) c.1619T>A (p.Val540Glu) n.2507T>A c.836T>A (p.Val279Glu) c.2030T>A (p.Val677Glu) | |
| 9 | g.91724456C>A | CA373796413 | ROR2 | c.2038G>T (p.Val680Leu) c.1618G>T (p.Val540Leu) n.2506G>T c.835G>T (p.Val279Leu) c.2029G>T (p.Val677Leu) | |
| 9 | g.91724456C>G | CA373796414 | ROR2 | c.2038G>C (p.Val680Leu) c.1618G>C (p.Val540Leu) n.2506G>C c.835G>C (p.Val279Leu) c.2029G>C (p.Val677Leu) | |
| 9 | g.91724456C>T | CA373796416 | ROR2 | c.2038G>A (p.Val680Met) c.1618G>A (p.Val540Met) n.2506G>A c.835G>A (p.Val279Met) c.2029G>A (p.Val677Met) | |
| 9 | g.91724457A>C | CA466339057 | ROR2 | c.2037T>G (p.Gly679=) c.1617T>G (p.Gly539=) n.2505T>G c.834T>G (p.Gly278=) c.2028T>G (p.Gly676=) | |
| 9 | g.91724457A>G | CA466339058 | ROR2 | c.2037T>C (p.Gly679=) c.1617T>C (p.Gly539=) n.2505T>C c.834T>C (p.Gly278=) c.2028T>C (p.Gly676=) | |
| 9 | g.91724457A>T | CA466339059 | ROR2 | c.2037T>A (p.Gly679=) c.1617T>A (p.Gly539=) n.2505T>A c.834T>A (p.Gly278=) c.2028T>A (p.Gly676=) | |
| 9 | g.91724458C>A | CA373796417 | ROR2 | c.2036G>T (p.Gly679Val) c.1616G>T (p.Gly539Val) n.2504G>T c.833G>T (p.Gly278Val) c.2027G>T (p.Gly676Val) | |
| 9 | g.91724458C>G | CA373796418 | ROR2 | c.2036G>C (p.Gly679Ala) c.1616G>C (p.Gly539Ala) n.2504G>C c.833G>C (p.Gly278Ala) c.2027G>C (p.Gly676Ala) | |
| 9 | g.91724458C>T | CA373796419 | ROR2 | c.2036G>A (p.Gly679Asp) c.1616G>A (p.Gly539Asp) n.2504G>A c.833G>A (p.Gly278Asp) c.2027G>A (p.Gly676Asp) | COSMIC |
| 9 | g.91724459C>A | CA373796420 | ROR2 | c.2035G>T (p.Gly679Cys) c.1615G>T (p.Gly539Cys) n.2503G>T c.832G>T (p.Gly278Cys) c.2026G>T (p.Gly676Cys) | |
| 9 | g.91724459C= | CA1863922795 | ROR2 | c.2035G= (p.Gly679=) c.1615G= (p.Gly539=) n.2503G= c.832G= (p.Gly278=) c.2026G= (p.Gly676=) | |
| 9 | g.91724459C>G | CA373796422 | ROR2 | c.2035G>C (p.Gly679Arg) c.1615G>C (p.Gly539Arg) n.2503G>C c.832G>C (p.Gly278Arg) c.2026G>C (p.Gly676Arg) | |
| 9 | g.91724459C>T | CA373796423 | ROR2 | c.2035G>A (p.Gly679Ser) c.1615G>A (p.Gly539Ser) n.2503G>A c.832G>A (p.Gly278Ser) c.2026G>A (p.Gly676Ser) | dbSNP gnomAD v4 COSMIC |
| 9 | g.91724460G>A | CA5120504 | ROR2 | c.2034C>T (p.Tyr678=) c.1614C>T (p.Tyr538=) n.2502C>T c.831C>T (p.Tyr277=) c.2025C>T (p.Tyr675=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.91724460G>C | CA373796426 | ROR2 | c.2034C>G (p.Tyr678Ter) c.1614C>G (p.Tyr538Ter) n.2502C>G c.831C>G (p.Tyr277Ter) c.2025C>G (p.Tyr675Ter) | |
| 9 | g.91724460G= | CA1863922798 | ROR2 | c.2034C= (p.Tyr678=) c.1614C= (p.Tyr538=) n.2502C= c.831C= (p.Tyr277=) c.2025C= (p.Tyr675=) | |
| 9 | g.91724460G>T | CA373796427 | ROR2 | c.2034C>A (p.Tyr678Ter) c.1614C>A (p.Tyr538Ter) n.2502C>A c.831C>A (p.Tyr277Ter) c.2025C>A (p.Tyr675Ter) | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.91724461T>A | CA373796434 | ROR2 | c.2033A>T (p.Tyr678Phe) c.1613A>T (p.Tyr538Phe) n.2501A>T c.830A>T (p.Tyr277Phe) c.2024A>T (p.Tyr675Phe) | |
| 9 | g.91724461T>C | CA373796430 | ROR2 | c.2033A>G (p.Tyr678Cys) c.1613A>G (p.Tyr538Cys) n.2501A>G c.830A>G (p.Tyr277Cys) c.2024A>G (p.Tyr675Cys) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.91724461T>G | CA373796429 | ROR2 | c.2033A>C (p.Tyr678Ser) c.1613A>C (p.Tyr538Ser) n.2501A>C c.830A>C (p.Tyr277Ser) c.2024A>C (p.Tyr675Ser) | |
| 9 | g.91724461T= | CA1863922800 | ROR2 | c.2033A= (p.Tyr678=) c.1613A= (p.Tyr538=) n.2501A= c.830A= (p.Tyr277=) c.2024A= (p.Tyr675=) | |
| 9 | g.91724462A>C | CA373796435 | ROR2 | c.2032T>G (p.Tyr678Asp) c.1612T>G (p.Tyr538Asp) n.2500T>G c.829T>G (p.Tyr277Asp) c.2023T>G (p.Tyr675Asp) | |
| 9 | g.91724462A>G | CA373796437 | ROR2 | c.2032T>C (p.Tyr678His) c.1612T>C (p.Tyr538His) n.2500T>C c.829T>C (p.Tyr277His) c.2023T>C (p.Tyr675His) | |
| 9 | g.91724462A>T | CA373796440 | ROR2 | c.2032T>A (p.Tyr678Asn) c.1612T>A (p.Tyr538Asn) n.2500T>A c.829T>A (p.Tyr277Asn) c.2023T>A (p.Tyr675Asn) | |
| 9 | g.91724463G>A | CA466339063 | ROR2 | c.2031C>T (p.Ser677=) c.1611C>T (p.Ser537=) n.2499C>T c.828C>T (p.Ser276=) c.2022C>T (p.Ser674=) | |
| 9 | g.91724463G>C | CA466339064 | ROR2 | c.2031C>G (p.Ser677=) c.1611C>G (p.Ser537=) n.2499C>G c.828C>G (p.Ser276=) c.2022C>G (p.Ser674=) | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.91724463G= | CA1863922802 | ROR2 | c.2031C= (p.Ser677=) c.1611C= (p.Ser537=) n.2499C= c.828C= (p.Ser276=) c.2022C= (p.Ser674=) | |
| 9 | g.91724463G>T | CA466339065 | ROR2 | c.2031C>A (p.Ser677=) c.1611C>A (p.Ser537=) n.2499C>A c.828C>A (p.Ser276=) c.2022C>A (p.Ser674=) | |
| 9 | g.91724464G>A | CA373796443 | ROR2 | c.2030C>T (p.Ser677Phe) c.1610C>T (p.Ser537Phe) n.2498C>T c.827C>T (p.Ser276Phe) c.2021C>T (p.Ser674Phe) | ClinVar dbSNP |
| 9 | g.91724464G>C | CA373796446 | ROR2 | c.2030C>G (p.Ser677Cys) c.1610C>G (p.Ser537Cys) n.2498C>G c.827C>G (p.Ser276Cys) c.2021C>G (p.Ser674Cys) | |
| 9 | g.91724464G>T | CA373796448 | ROR2 | c.2030C>A (p.Ser677Tyr) c.1610C>A (p.Ser537Tyr) n.2498C>A c.827C>A (p.Ser276Tyr) c.2021C>A (p.Ser674Tyr) | |
| 9 | g.91724465A>C | CA373796449 | ROR2 | c.2029T>G (p.Ser677Ala) c.1609T>G (p.Ser537Ala) n.2497T>G c.826T>G (p.Ser276Ala) c.2020T>G (p.Ser674Ala) | |
| 9 | g.91724465A>G | CA373796451 | ROR2 | c.2029T>C (p.Ser677Pro) c.1609T>C (p.Ser537Pro) n.2497T>C c.826T>C (p.Ser276Pro) c.2020T>C (p.Ser674Pro) | COSMIC |
| 9 | g.91724465A>T | CA373796454 | ROR2 | c.2029T>A (p.Ser677Thr) c.1609T>A (p.Ser537Thr) n.2497T>A c.826T>A (p.Ser276Thr) c.2020T>A (p.Ser674Thr) | |
| 9 | g.91724466C>A | CA373796455 | ROR2 | c.2028G>T (p.Trp676Cys) c.1608G>T (p.Trp536Cys) n.2496G>T c.825G>T (p.Trp275Cys) c.2019G>T (p.Trp673Cys) | |
| 9 | g.91724466C>G | CA373796460 | ROR2 | c.2028G>C (p.Trp676Cys) c.1608G>C (p.Trp536Cys) n.2496G>C c.825G>C (p.Trp275Cys) c.2019G>C (p.Trp673Cys) | |
| 9 | g.91724466C>T | CA373796462 | ROR2 | c.2028G>A (p.Trp676Ter) c.1608G>A (p.Trp536Ter) n.2496G>A c.825G>A (p.Trp275Ter) c.2019G>A (p.Trp673Ter) | |
| 9 | g.91724467C>A | CA373796466 | ROR2 | c.2027G>T (p.Trp676Leu) c.1607G>T (p.Trp536Leu) n.2495G>T c.824G>T (p.Trp275Leu) c.2018G>T (p.Trp673Leu) | |
| 9 | g.91724467C>G | CA373796463 | ROR2 | c.2027G>C (p.Trp676Ser) c.1607G>C (p.Trp536Ser) n.2495G>C c.824G>C (p.Trp275Ser) c.2018G>C (p.Trp673Ser) | |
| 9 | g.91724467C>T | CA373796465 | ROR2 | c.2027G>A (p.Trp676Ter) c.1607G>A (p.Trp536Ter) n.2495G>A c.824G>A (p.Trp275Ter) c.2018G>A (p.Trp673Ter) | gnomAD v4 |