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 |
|---|---|---|---|---|---|
| 21 | g.18312975G>A | CA409849000 | TMPRSS15 | c.2135C>T (p.Ser712Leu) c.2270C>T (p.Ser757Leu) c.2225C>T (p.Ser742Leu) c.2189C>T (p.Ser730Leu) c.2180C>T (p.Ser727Leu) | |
| 21 | g.18312975G>C | CA116666 | TMPRSS15 | c.2135C>G (p.Ser712Ter) c.2270C>G (p.Ser757Ter) c.2225C>G (p.Ser742Ter) c.2189C>G (p.Ser730Ter) c.2180C>G (p.Ser727Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 21 | g.18312975G= | CA2379751705 | TMPRSS15 | c.2135C= (p.Ser712=) c.2270C= (p.Ser757=) c.2225C= (p.Ser742=) c.2189C= (p.Ser730=) c.2180C= (p.Ser727=) | |
| 21 | g.18312975G>T | CA409849001 | TMPRSS15 | c.2135C>A (p.Ser712Ter) c.2270C>A (p.Ser757Ter) c.2225C>A (p.Ser742Ter) c.2189C>A (p.Ser730Ter) c.2180C>A (p.Ser727Ter) | gnomAD v4 |
| 21 | g.18312976A>C | CA409849002 | TMPRSS15 | c.2134T>G (p.Ser712Ala) c.2269T>G (p.Ser757Ala) c.2224T>G (p.Ser742Ala) c.2188T>G (p.Ser730Ala) c.2179T>G (p.Ser727Ala) | |
| 21 | g.18312976A>G | CA409849003 | TMPRSS15 | c.2134T>C (p.Ser712Pro) c.2269T>C (p.Ser757Pro) c.2224T>C (p.Ser742Pro) c.2188T>C (p.Ser730Pro) c.2179T>C (p.Ser727Pro) | |
| 21 | g.18312976A>T | CA409849004 | TMPRSS15 | c.2134T>A (p.Ser712Thr) c.2269T>A (p.Ser757Thr) c.2224T>A (p.Ser742Thr) c.2188T>A (p.Ser730Thr) c.2179T>A (p.Ser727Thr) | |
| 21 | g.18312977A>C | CA409849005 | TMPRSS15 | c.2133T>G (p.Ile711Met) c.2268T>G (p.Ile756Met) c.2223T>G (p.Ile741Met) c.2187T>G (p.Ile729Met) c.2178T>G (p.Ile726Met) | |
| 21 | g.18312977A>G | CA511460493 | TMPRSS15 | c.2133T>C (p.Ile711=) c.2268T>C (p.Ile756=) c.2223T>C (p.Ile741=) c.2187T>C (p.Ile729=) c.2178T>C (p.Ile726=) | |
| 21 | g.18312977A>T | CA511460494 | TMPRSS15 | c.2133T>A (p.Ile711=) c.2268T>A (p.Ile756=) c.2223T>A (p.Ile741=) c.2187T>A (p.Ile729=) c.2178T>A (p.Ile726=) | |
| 21 | g.18312978A>C | CA409849006 | TMPRSS15 | c.2132T>G (p.Ile711Ser) c.2267T>G (p.Ile756Ser) c.2222T>G (p.Ile741Ser) c.2186T>G (p.Ile729Ser) c.2177T>G (p.Ile726Ser) | |
| 21 | g.18312978A>G | CA409849007 | TMPRSS15 | c.2132T>C (p.Ile711Thr) c.2267T>C (p.Ile756Thr) c.2222T>C (p.Ile741Thr) c.2186T>C (p.Ile729Thr) c.2177T>C (p.Ile726Thr) | |
| 21 | g.18312978A>T | CA409849008 | TMPRSS15 | c.2132T>A (p.Ile711Asn) c.2267T>A (p.Ile756Asn) c.2222T>A (p.Ile741Asn) c.2186T>A (p.Ile729Asn) c.2177T>A (p.Ile726Asn) | |
| 21 | g.18312979T>A | CA409849010 | TMPRSS15 | c.2131A>T (p.Ile711Phe) c.2266A>T (p.Ile756Phe) c.2221A>T (p.Ile741Phe) c.2185A>T (p.Ile729Phe) c.2176A>T (p.Ile726Phe) | |
| 21 | g.18312979T>C | CA9984190 | TMPRSS15 | c.2131A>G (p.Ile711Val) c.2266A>G (p.Ile756Val) c.2221A>G (p.Ile741Val) c.2185A>G (p.Ile729Val) c.2176A>G (p.Ile726Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 21 | g.18312979T>G | CA409849009 | TMPRSS15 | c.2131A>C (p.Ile711Leu) c.2266A>C (p.Ile756Leu) c.2221A>C (p.Ile741Leu) c.2185A>C (p.Ile729Leu) c.2176A>C (p.Ile726Leu) | |
| 21 | g.18312979T= | CA2379751707 | TMPRSS15 | c.2131A= (p.Ile711=) c.2266A= (p.Ile756=) c.2221A= (p.Ile741=) c.2185A= (p.Ile729=) c.2176A= (p.Ile726=) | |
| 21 | g.18312980C>A | CA409849012 | TMPRSS15 | c.2130G>T (p.Gln710His) c.2265G>T (p.Gln755His) c.2220G>T (p.Gln740His) c.2184G>T (p.Gln728His) c.2175G>T (p.Gln725His) | |
| 21 | g.18312980C= | CA2379751709 | TMPRSS15 | c.2130G= (p.Gln710=) c.2265G= (p.Gln755=) c.2220G= (p.Gln740=) c.2184G= (p.Gln728=) c.2175G= (p.Gln725=) | |
| 21 | g.18312980C>G | CA409849011 | TMPRSS15 | c.2130G>C (p.Gln710His) c.2265G>C (p.Gln755His) c.2220G>C (p.Gln740His) c.2184G>C (p.Gln728His) c.2175G>C (p.Gln725His) | |
| 21 | g.18312980C>T | CA511460498 | TMPRSS15 | c.2130G>A (p.Gln710=) c.2265G>A (p.Gln755=) c.2220G>A (p.Gln740=) c.2184G>A (p.Gln728=) c.2175G>A (p.Gln725=) | dbSNP gnomAD v2 gnomAD v4 |
| 21 | g.18312981T>A | CA409849013 | TMPRSS15 | c.2129A>T (p.Gln710Leu) c.2264A>T (p.Gln755Leu) c.2219A>T (p.Gln740Leu) c.2183A>T (p.Gln728Leu) c.2174A>T (p.Gln725Leu) | |
| 21 | g.18312981T>C | CA409849014 | TMPRSS15 | c.2129A>G (p.Gln710Arg) c.2264A>G (p.Gln755Arg) c.2219A>G (p.Gln740Arg) c.2183A>G (p.Gln728Arg) c.2174A>G (p.Gln725Arg) | gnomAD v4 |
| 21 | g.18312981T>G | CA409849015 | TMPRSS15 | c.2129A>C (p.Gln710Pro) c.2264A>C (p.Gln755Pro) c.2219A>C (p.Gln740Pro) c.2183A>C (p.Gln728Pro) c.2174A>C (p.Gln725Pro) | |
| 21 | g.18312982G>A | CA409849016 | TMPRSS15 | c.2128C>T (p.Gln710Ter) c.2263C>T (p.Gln755Ter) c.2218C>T (p.Gln740Ter) c.2182C>T (p.Gln728Ter) c.2173C>T (p.Gln725Ter) | ClinVar gnomAD v4 |
| 21 | g.18312982G>C | CA409849017 | TMPRSS15 | c.2128C>G (p.Gln710Glu) c.2263C>G (p.Gln755Glu) c.2218C>G (p.Gln740Glu) c.2182C>G (p.Gln728Glu) c.2173C>G (p.Gln725Glu) | gnomAD v4 |
| 21 | g.18312982G>T | CA409849018 | TMPRSS15 | c.2128C>A (p.Gln710Lys) c.2263C>A (p.Gln755Lys) c.2218C>A (p.Gln740Lys) c.2182C>A (p.Gln728Lys) c.2173C>A (p.Gln725Lys) | COSMIC |
| 21 | g.18312984dup | CA2654083896 | TMPRSS15 | c.2128dup (p.Gln710ProfsTer5) c.2263dup (p.Gln755ProfsTer5) c.2218dup (p.Gln740ProfsTer5) c.2182dup (p.Gln728ProfsTer5) c.2173dup (p.Gln725ProfsTer5) | gnomAD v4 |
| 21 | g.18312983G>A | CA511460502 | TMPRSS15 | c.2127C>T (p.Thr709=) c.2262C>T (p.Thr754=) c.2217C>T (p.Thr739=) c.2181C>T (p.Thr727=) c.2172C>T (p.Thr724=) | |
| 21 | g.18312983G>C | CA511460505 | TMPRSS15 | c.2127C>G (p.Thr709=) c.2262C>G (p.Thr754=) c.2217C>G (p.Thr739=) c.2181C>G (p.Thr727=) c.2172C>G (p.Thr724=) | |
| 21 | g.18312983G>T | CA511460503 | TMPRSS15 | c.2127C>A (p.Thr709=) c.2262C>A (p.Thr754=) c.2217C>A (p.Thr739=) c.2181C>A (p.Thr727=) c.2172C>A (p.Thr724=) | |
| 21 | g.18312984G>A | CA409849019 | TMPRSS15 | c.2126C>T (p.Thr709Ile) c.2261C>T (p.Thr754Ile) c.2216C>T (p.Thr739Ile) c.2180C>T (p.Thr727Ile) c.2171C>T (p.Thr724Ile) | dbSNP gnomAD v4 |
| 21 | g.18312984G>C | CA409849020 | TMPRSS15 | c.2126C>G (p.Thr709Ser) c.2261C>G (p.Thr754Ser) c.2216C>G (p.Thr739Ser) c.2180C>G (p.Thr727Ser) c.2171C>G (p.Thr724Ser) | |
| 21 | g.18312984G>T | CA409849021 | TMPRSS15 | c.2126C>A (p.Thr709Asn) c.2261C>A (p.Thr754Asn) c.2216C>A (p.Thr739Asn) c.2180C>A (p.Thr727Asn) c.2171C>A (p.Thr724Asn) | |
| 21 | g.18312985T>A | CA409849022 | TMPRSS15 | c.2125A>T (p.Thr709Ser) c.2260A>T (p.Thr754Ser) c.2215A>T (p.Thr739Ser) c.2179A>T (p.Thr727Ser) c.2170A>T (p.Thr724Ser) | |
| 21 | g.18312985T>C | CA409849023 | TMPRSS15 | c.2125A>G (p.Thr709Ala) c.2260A>G (p.Thr754Ala) c.2215A>G (p.Thr739Ala) c.2179A>G (p.Thr727Ala) c.2170A>G (p.Thr724Ala) | gnomAD v4 |
| 21 | g.18312985T>G | CA409849024 | TMPRSS15 | c.2125A>C (p.Thr709Pro) c.2260A>C (p.Thr754Pro) c.2215A>C (p.Thr739Pro) c.2179A>C (p.Thr727Pro) c.2170A>C (p.Thr724Pro) | |
| 21 | g.18312986G>A | CA511460609 | TMPRSS15 | c.2124C>T (p.Thr708=) c.2259C>T (p.Thr753=) c.2214C>T (p.Thr738=) c.2178C>T (p.Thr726=) c.2169C>T (p.Thr723=) | |
| 21 | g.18312986G>C | CA511460610 | TMPRSS15 | c.2124C>G (p.Thr708=) c.2259C>G (p.Thr753=) c.2214C>G (p.Thr738=) c.2178C>G (p.Thr726=) c.2169C>G (p.Thr723=) | |
| 21 | g.18312986G>T | CA511460611 | TMPRSS15 | c.2124C>A (p.Thr708=) c.2259C>A (p.Thr753=) c.2214C>A (p.Thr738=) c.2178C>A (p.Thr726=) c.2169C>A (p.Thr723=) | |
| 21 | g.18312987G>A | CA409849027 | TMPRSS15 | c.2123C>T (p.Thr708Ile) c.2258C>T (p.Thr753Ile) c.2213C>T (p.Thr738Ile) c.2177C>T (p.Thr726Ile) c.2168C>T (p.Thr723Ile) | gnomAD v4 |
| 21 | g.18312987G>C | CA409849025 | TMPRSS15 | c.2123C>G (p.Thr708Ser) c.2258C>G (p.Thr753Ser) c.2213C>G (p.Thr738Ser) c.2177C>G (p.Thr726Ser) c.2168C>G (p.Thr723Ser) | |
| 21 | g.18312987G>T | CA409849026 | TMPRSS15 | c.2123C>A (p.Thr708Asn) c.2258C>A (p.Thr753Asn) c.2213C>A (p.Thr738Asn) c.2177C>A (p.Thr726Asn) c.2168C>A (p.Thr723Asn) | |
| 21 | g.18312988T>A | CA409849028 | TMPRSS15 | c.2122A>T (p.Thr708Ser) c.2257A>T (p.Thr753Ser) c.2212A>T (p.Thr738Ser) c.2176A>T (p.Thr726Ser) c.2167A>T (p.Thr723Ser) | |
| 21 | g.18312988T>C | CA409849029 | TMPRSS15 | c.2122A>G (p.Thr708Ala) c.2257A>G (p.Thr753Ala) c.2212A>G (p.Thr738Ala) c.2176A>G (p.Thr726Ala) c.2167A>G (p.Thr723Ala) | |
| 21 | g.18312988T>G | CA409849030 | TMPRSS15 | c.2122A>C (p.Thr708Pro) c.2257A>C (p.Thr753Pro) c.2212A>C (p.Thr738Pro) c.2176A>C (p.Thr726Pro) c.2167A>C (p.Thr723Pro) | |
| 21 | g.18312989C>A | CA409849031 | TMPRSS15 | c.2121G>T (p.Trp707Cys) c.2256G>T (p.Trp752Cys) c.2211G>T (p.Trp737Cys) c.2175G>T (p.Trp725Cys) c.2166G>T (p.Trp722Cys) | |
| 21 | g.18312989C>G | CA409849032 | TMPRSS15 | c.2121G>C (p.Trp707Cys) c.2256G>C (p.Trp752Cys) c.2211G>C (p.Trp737Cys) c.2175G>C (p.Trp725Cys) c.2166G>C (p.Trp722Cys) | |
| 21 | g.18312989C>T | CA409849033 | TMPRSS15 | c.2121G>A (p.Trp707Ter) c.2256G>A (p.Trp752Ter) c.2211G>A (p.Trp737Ter) c.2175G>A (p.Trp725Ter) c.2166G>A (p.Trp722Ter) | |
| 21 | g.18312990C>A | CA409849034 | TMPRSS15 | c.2120G>T (p.Trp707Leu) c.2255G>T (p.Trp752Leu) c.2210G>T (p.Trp737Leu) c.2174G>T (p.Trp725Leu) c.2165G>T (p.Trp722Leu) | gnomAD v4 |