Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.22125654G>A | CA4662446 | HR | c.1484C>T (p.Ala495Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.22125654G>C | CA10630653 | HR | c.1484C>G (p.Ala495Gly) | ClinVar dbSNP |
8 | g.22125654G= | CA1770271924 | HR | c.1484C= (p.Ala495=) | |
8 | g.22125654G>T | CA370496184 | HR | c.1484C>A (p.Ala495Asp) | |
8 | g.22125655C>A | CA370496187 | HR | c.1483G>T (p.Ala495Ser) | |
8 | g.22125655C>G | CA370496188 | HR | c.1483G>C (p.Ala495Pro) | |
8 | g.22125655C>T | CA370496190 | HR | c.1483G>A (p.Ala495Thr) | gnomAD v4 |
8 | g.22125656C>A | CA459893316 | HR | c.1482G>T (p.Leu494=) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.22125656C= | CA1770271933 | HR | c.1482G= (p.Leu494=) | |
8 | g.22125656C>G | CA459893314 | HR | c.1482G>C (p.Leu494=) | gnomAD v4 |
8 | g.22125656C>T | CA459893315 | HR | c.1482G>A (p.Leu494=) | |
8 | g.22125657A>C | CA370496206 | HR | c.1481T>G (p.Leu494Arg) | gnomAD v4 |
8 | g.22125657A>G | CA370496204 | HR | c.1481T>C (p.Leu494Pro) | |
8 | g.22125657A>T | CA370496201 | HR | c.1481T>A (p.Leu494Gln) | |
8 | g.22125658G>A | CA459893318 | HR | c.1480C>T (p.Leu494=) | gnomAD v4 |
8 | g.22125658G>C | CA370496209 | HR | c.1480C>G (p.Leu494Val) | |
8 | g.22125658G>T | CA370496210 | HR | c.1480C>A (p.Leu494Met) | |
8 | g.22125659T>A | CA370496218 | HR | c.1479A>T (p.Lys493Asn) | |
8 | g.22125659T>C | CA459893320 | HR | c.1479A>G (p.Lys493=) | |
8 | g.22125659T>G | CA370496220 | HR | c.1479A>C (p.Lys493Asn) | |
8 | g.22125660T>A | CA370496223 | HR | c.1478A>T (p.Lys493Ile) | |
8 | g.22125660T>C | CA370496226 | HR | c.1478A>G (p.Lys493Arg) | |
8 | g.22125660T>G | CA370496227 | HR | c.1478A>C (p.Lys493Thr) | |
8 | g.22125661T>A | CA370496230 | HR | c.1477A>T (p.Lys493Ter) | |
8 | g.22125661T>C | CA4662447 | HR | c.1477A>G (p.Lys493Glu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.22125661T>G | CA370496232 | HR | c.1477A>C (p.Lys493Gln) | |
8 | g.22125661T= | CA1770271934 | HR | c.1477A= (p.Lys493=) | |
8 | g.22125662T>A | CA459893322 | HR | c.1476A>T (p.Ala492=) | |
8 | g.22125662T>C | CA459893323 | HR | c.1476A>G (p.Ala492=) | gnomAD v4 |
8 | g.22125662T>G | CA459893324 | HR | c.1476A>C (p.Ala492=) | |
8 | g.22125663G>A | CA370496235 | HR | c.1475C>T (p.Ala492Val) | COSMIC |
8 | g.22125663G>C | CA370496236 | HR | c.1475C>G (p.Ala492Gly) | |
8 | g.22125663G= | CA1770271939 | HR | c.1475C= (p.Ala492=) | |
8 | g.22125663G>T | CA4662448 | HR | c.1475C>A (p.Ala492Glu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.22125664C>A | CA4662450 | HR | c.1474G>T (p.Ala492Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.22125664C= | CA1770271944 | HR | c.1474G= (p.Ala492=) | |
8 | g.22125664C>G | CA370496239 | HR | c.1474G>C (p.Ala492Pro) | |
8 | g.22125664C>T | CA4662449 | HR | c.1474G>A (p.Ala492Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.22125665A>C | CA459893327 | HR | c.1473T>G (p.Pro491=) | |
8 | g.22125665A>G | CA459893328 | HR | c.1473T>C (p.Pro491=) | |
8 | g.22125665A>T | CA459893329 | HR | c.1473T>A (p.Pro491=) | |
8 | g.22125666G>A | CA370496242 | HR | c.1472C>T (p.Pro491Leu) | |
8 | g.22125666G>C | CA370496243 | HR | c.1472C>G (p.Pro491Arg) | |
8 | g.22125666G>T | CA370496244 | HR | c.1472C>A (p.Pro491His) | |
8 | g.22125667G>A | CA370496245 | HR | c.1471C>T (p.Pro491Ser) | gnomAD v4 |
8 | g.22125667G>C | CA370496246 | HR | c.1471C>G (p.Pro491Ala) | |
8 | g.22125667G>T | CA370496247 | HR | c.1471C>A (p.Pro491Thr) | |
8 | g.22125668G>A | CA459893332 | HR | c.1470C>T (p.Leu490=) | |
8 | g.22125668G>C | CA459893333 | HR | c.1470C>G (p.Leu490=) | |
8 | g.22125668G>T | CA459893334 | HR | c.1470C>A (p.Leu490=) |