| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.127814982_127820052del | CA1139659920 | ClinVar | ||
| 9 | g.127816024_127816026del | CA2691805857 | ENG | c.1226_1228del (p.Ala409del) c.1772_1774del (p.Ala591del) | gnomAD v4 |
| 9 | g.127816025G>A | CA5252630 | ENG | c.1224C>T (p.Pro408=) c.1770C>T (p.Pro590=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.127816025G>C | CA467474532 | ENG | c.1224C>G (p.Pro408=) c.1770C>G (p.Pro590=) | |
| 9 | g.127816025G= | CA1879981936 | ENG | c.1224C= (p.Pro408=) c.1770C= (p.Pro590=) | |
| 9 | g.127816025G>T | CA467474533 | ENG | c.1224C>A (p.Pro408=) c.1770C>A (p.Pro590=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.127816026G>A | CA374972217 | ENG | c.1223C>T (p.Pro408Leu) c.1769C>T (p.Pro590Leu) | gnomAD v4 |
| 9 | g.127816026G>C | CA374972219 | ENG | c.1223C>G (p.Pro408Arg) c.1769C>G (p.Pro590Arg) | gnomAD v4 |
| 9 | g.127816026G= | CA1879981943 | ENG | c.1223C= (p.Pro408=) c.1769C= (p.Pro590=) | |
| 9 | g.127816026G>T | CA374972221 | ENG | c.1223C>A (p.Pro408His) c.1769C>A (p.Pro590His) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.127816027G>A | CA374972231 | ENG | c.1222C>T (p.Pro408Ser) c.1768C>T (p.Pro590Ser) | gnomAD v4 |
| 9 | g.127816027G>C | CA374972229 | ENG | c.1222C>G (p.Pro408Ala) c.1768C>G (p.Pro590Ala) | |
| 9 | g.127816027G>T | CA374972226 | ENG | c.1222C>A (p.Pro408Thr) c.1768C>A (p.Pro590Thr) | |
| 9 | g.127816028C>A | CA467474536 | ENG | c.1221G>T (p.Leu407=) c.1767G>T (p.Leu589=) | |
| 9 | g.127816028C= | CA1879981947 | ENG | c.1221G= (p.Leu407=) c.1767G= (p.Leu589=) | |
| 9 | g.127816028C>G | CA467474537 | ENG | c.1221G>C (p.Leu407=) c.1767G>C (p.Leu589=) | |
| 9 | g.127816028C>T | CA467474538 | ENG | c.1221G>A (p.Leu407=) c.1767G>A (p.Leu589=) | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.127816029A= | CA1879981952 | ENG | c.1220T= (p.Leu407=) c.1766T= (p.Leu589=) | |
| 9 | g.127816029A>C | CA374972243 | ENG | c.1220T>G (p.Leu407Arg) c.1766T>G (p.Leu589Arg) | |
| 9 | g.127816029A>G | CA5252631 | ENG | c.1220T>C (p.Leu407Pro) c.1766T>C (p.Leu589Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.127816029A>T | CA374972247 | ENG | c.1220T>A (p.Leu407Gln) c.1766T>A (p.Leu589Gln) | |
| 9 | g.127816030G>A | CA467474539 | ENG | c.1219C>T (p.Leu407=) c.1765C>T (p.Leu589=) | gnomAD v4 |
| 9 | g.127816030G>C | CA374972252 | ENG | c.1219C>G (p.Leu407Val) c.1765C>G (p.Leu589Val) | |
| 9 | g.127816030G>T | CA374972255 | ENG | c.1219C>A (p.Leu407Met) c.1765C>A (p.Leu589Met) | |
| 9 | g.127816031G>A | CA467474542 | ENG | c.1218C>T (p.Val406=) c.1764C>T (p.Val588=) | gnomAD v4 |
| 9 | g.127816031G>C | CA467474544 | ENG | c.1218C>G (p.Val406=) c.1764C>G (p.Val588=) | |
| 9 | g.127816031G>T | CA467474547 | ENG | c.1218C>A (p.Val406=) c.1764C>A (p.Val588=) | gnomAD v4 |
| 9 | g.127816032A>C | CA374972257 | ENG | c.1217T>G (p.Val406Gly) c.1763T>G (p.Val588Gly) | |
| 9 | g.127816032A>G | CA374972259 | ENG | c.1217T>C (p.Val406Ala) c.1763T>C (p.Val588Ala) | |
| 9 | g.127816032A>T | CA374972262 | ENG | c.1217T>A (p.Val406Asp) c.1763T>A (p.Val588Asp) | |
| 9 | g.127816033C>A | CA374972265 | ENG | c.1216G>T (p.Val406Phe) c.1762G>T (p.Val588Phe) | |
| 9 | g.127816033C= | CA1879981958 | ENG | c.1216G= (p.Val406=) c.1762G= (p.Val588=) | |
| 9 | g.127816033C>G | CA374972267 | ENG | c.1216G>C (p.Val406Leu) c.1762G>C (p.Val588Leu) | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.127816033C>T | CA5252632 | ENG | c.1216G>A (p.Val406Ile) c.1762G>A (p.Val588Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.127816034G>A | CA5252633 | ENG | c.1215C>T (p.Leu405=) c.1761C>T (p.Leu587=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.127816034G>C | CA467474552 | ENG | c.1215C>G (p.Leu405=) c.1761C>G (p.Leu587=) | gnomAD v4 |
| 9 | g.127816034G= | CA1879981966 | ENG | c.1215C= (p.Leu405=) c.1761C= (p.Leu587=) | |
| 9 | g.127816034G>T | CA467474554 | ENG | c.1215C>A (p.Leu405=) c.1761C>A (p.Leu587=) | gnomAD v4 |
| 9 | g.127816035A>C | CA374972273 | ENG | c.1214T>G (p.Leu405Arg) c.1760T>G (p.Leu587Arg) | |
| 9 | g.127816035A>G | CA374972274 | ENG | c.1214T>C (p.Leu405Pro) c.1760T>C (p.Leu587Pro) | |
| 9 | g.127816035A>T | CA374972272 | ENG | c.1214T>A (p.Leu405His) c.1760T>A (p.Leu587His) | |
| 9 | g.127816036G>A | CA5252634 | ENG | c.1213C>T (p.Leu405Phe) c.1759C>T (p.Leu587Phe) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.127816036G>C | CA374972277 | ENG | c.1213C>G (p.Leu405Val) c.1759C>G (p.Leu587Val) | |
| 9 | g.127816036G= | CA1879981974 | ENG | c.1213C= (p.Leu405=) c.1759C= (p.Leu587=) | |
| 9 | g.127816036G>T | CA374972279 | ENG | c.1213C>A (p.Leu405Ile) c.1759C>A (p.Leu587Ile) | |
| 9 | g.127816037G>A | CA5252635 | ENG | c.1212C>T (p.Gly404=) c.1758C>T (p.Gly586=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.127816037G>C | CA467474562 | ENG | c.1212C>G (p.Gly404=) c.1758C>G (p.Gly586=) | gnomAD v4 |
| 9 | g.127816037G= | CA1879981983 | ENG | c.1212C= (p.Gly404=) c.1758C= (p.Gly586=) | |
| 9 | g.127816037G>T | CA467474563 | ENG | c.1212C>A (p.Gly404=) c.1758C>A (p.Gly586=) | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.127816038C>A | CA374972282 | ENG | c.1211G>T (p.Gly404Val) c.1757G>T (p.Gly586Val) | gnomAD v4 COSMIC COSMIC |