Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.99851537G>A | CA5644184 | ABCC2 | c.4544G>A (p.Cys1515Tyr) c.614G>A c.3848G>A (p.Cys1283Tyr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.99851537G>C | CA378130687 | ABCC2 | c.4544G>C (p.Cys1515Ser) c.614G>C c.3848G>C (p.Cys1283Ser) | |
10 | g.99851537G= | CA1931484653 | ABCC2 | c.4544G= (p.Cys1515=) c.614G= c.3848G= (p.Cys1283=) | |
10 | g.99851537G>T | CA378130688 | ABCC2 | c.4544G>T (p.Cys1515Phe) c.614G>T c.3848G>T (p.Cys1283Phe) | |
10 | g.99851538C>A | CA378130692 | ABCC2 | c.4545C>A (p.Cys1515Ter) c.615C>A c.3849C>A (p.Cys1283Ter) | |
10 | g.99851538C= | CA1931484663 | ABCC2 | c.4545C= (p.Cys1515=) c.615C= c.3849C= (p.Cys1283=) | |
10 | g.99851538C>G | CA378130690 | ABCC2 | c.4545C>G (p.Cys1515Trp) c.615C>G c.3849C>G (p.Cys1283Trp) | |
10 | g.99851538C>T | CA5644185 | ABCC2 | c.4545C>T (p.Cys1515=) c.615C>T c.3849C>T (p.Cys1283=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
10 | g.99851539G>A | CA5644186 | ABCC2 | c.4546G>A (p.Gly1516Ser) c.616G>A c.3850G>A (p.Gly1284Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.99851539G>C | CA378130695 | ABCC2 | c.4546G>C (p.Gly1516Arg) c.616G>C c.3850G>C (p.Gly1284Arg) | |
10 | g.99851539G= | CA1931484667 | ABCC2 | c.4546G= (p.Gly1516=) c.616G= c.3850G= (p.Gly1284=) | |
10 | g.99851539G>T | CA378130698 | ABCC2 | c.4546G>T (p.Gly1516Cys) c.616G>T c.3850G>T (p.Gly1284Cys) | |
10 | g.99851540G>A | CA378130701 | ABCC2 | c.4547G>A (p.Gly1516Asp) c.617G>A c.3851G>A (p.Gly1284Asp) | dbSNP gnomAD v4 |
10 | g.99851540G>C | CA378130702 | ABCC2 | c.4547G>C (p.Gly1516Ala) c.617G>C c.3851G>C (p.Gly1284Ala) | |
10 | g.99851540G>T | CA378130704 | ABCC2 | c.4547G>T (p.Gly1516Val) c.617G>T c.3851G>T (p.Gly1284Val) | |
10 | g.99851541C>A | CA471136052 | ABCC2 | c.4548C>A (p.Gly1516=) c.618C>A c.3852C>A (p.Gly1284=) | |
10 | g.99851541C>G | CA471136053 | ABCC2 | c.4548C>G (p.Gly1516=) c.618C>G c.3852C>G (p.Gly1284=) | |
10 | g.99851541C>T | CA471136054 | ABCC2 | c.4548C>T (p.Gly1516=) c.618C>T c.3852C>T (p.Gly1284=) | |
10 | g.99851542A>C | CA378130706 | ABCC2 | c.4549A>C (p.Ser1517Arg) c.619A>C c.3853A>C (p.Ser1285Arg) | |
10 | g.99851542A>G | CA378130711 | ABCC2 | c.4549A>G (p.Ser1517Gly) c.619A>G c.3853A>G (p.Ser1285Gly) | |
10 | g.99851542A>T | CA378130709 | ABCC2 | c.4549A>T (p.Ser1517Cys) c.619A>T c.3853A>T (p.Ser1285Cys) | |
10 | g.99851543G>A | CA378130713 | ABCC2 | c.4550G>A (p.Ser1517Asn) c.620G>A c.3854G>A (p.Ser1285Asn) | dbSNP |
10 | g.99851543G>C | CA378130714 | ABCC2 | c.4550G>C (p.Ser1517Thr) c.620G>C c.3854G>C (p.Ser1285Thr) | |
10 | g.99851543G>T | CA378130717 | ABCC2 | c.4550G>T (p.Ser1517Ile) c.620G>T c.3854G>T (p.Ser1285Ile) | gnomAD v4 |
10 | g.99851544C>A | CA378130719 | ABCC2 | c.4551C>A (p.Ser1517Arg) c.621C>A c.3855C>A (p.Ser1285Arg) | |
10 | g.99851544C>G | CA378130722 | ABCC2 | c.4551C>G (p.Ser1517Arg) c.621C>G c.3855C>G (p.Ser1285Arg) | |
10 | g.99851544C>T | CA471136055 | ABCC2 | c.4551C>T (p.Ser1517=) c.621C>T c.3855C>T (p.Ser1285=) | dbSNP |
10 | g.99851545C>A | CA378130725 | ABCC2 | c.4552C>A (p.Pro1518Thr) c.622C>A c.3856C>A (p.Pro1286Thr) | |
10 | g.99851545C>G | CA378130727 | ABCC2 | c.4552C>G (p.Pro1518Ala) c.622C>G c.3856C>G (p.Pro1286Ala) | gnomAD v4 |
10 | g.99851545C>T | CA378130728 | ABCC2 | c.4552C>T (p.Pro1518Ser) c.622C>T c.3856C>T (p.Pro1286Ser) | gnomAD v4 |
10 | g.99851546C>A | CA378130730 | ABCC2 | c.4553C>A (p.Pro1518His) c.623C>A c.3857C>A (p.Pro1286His) | |
10 | g.99851546C= | CA1931484673 | ABCC2 | c.4553C= (p.Pro1518=) c.623C= c.3857C= (p.Pro1286=) | |
10 | g.99851546C>G | CA5644187 | ABCC2 | c.4553C>G (p.Pro1518Arg) c.623C>G c.3857C>G (p.Pro1286Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.99851546C>T | CA378130734 | ABCC2 | c.4553C>T (p.Pro1518Leu) c.623C>T c.3857C>T (p.Pro1286Leu) | |
10 | g.99851547T>A | CA471136058 | ABCC2 | c.4554T>A (p.Pro1518=) c.624T>A c.3858T>A (p.Pro1286=) | |
10 | g.99851547T>C | CA471136057 | ABCC2 | c.4554T>C (p.Pro1518=) c.624T>C c.3858T>C (p.Pro1286=) | |
10 | g.99851547T>G | CA471136056 | ABCC2 | c.4554T>G (p.Pro1518=) c.624T>G c.3858T>G (p.Pro1286=) | |
10 | g.99851548G>A | CA378130737 | ABCC2 | c.4555G>A (p.Glu1519Lys) c.625G>A c.3859G>A (p.Glu1287Lys) | ClinVar dbSNP |
10 | g.99851548G>C | CA378130741 | ABCC2 | c.4555G>C (p.Glu1519Gln) c.625G>C c.3859G>C (p.Glu1287Gln) | |
10 | g.99851548G= | CA1931484683 | ABCC2 | c.4555G= (p.Glu1519=) c.625G= c.3859G= (p.Glu1287=) | |
10 | g.99851548G>T | CA378130739 | ABCC2 | c.4555G>T (p.Glu1519Ter) c.625G>T c.3859G>T (p.Glu1287Ter) | |
10 | g.99851549A>C | CA378130743 | ABCC2 | c.4556A>C (p.Glu1519Ala) c.626A>C c.3860A>C (p.Glu1287Ala) | |
10 | g.99851549A>G | CA378130746 | ABCC2 | c.4556A>G (p.Glu1519Gly) c.626A>G c.3860A>G (p.Glu1287Gly) | gnomAD v4 |
10 | g.99851549A>T | CA378130745 | ABCC2 | c.4556A>T (p.Glu1519Val) c.626A>T c.3860A>T (p.Glu1287Val) | |
10 | g.99851550A= | CA1931484698 | ABCC2 | c.4557A= (p.Glu1519=) c.627A= c.3861A= (p.Glu1287=) | |
10 | g.99851550A>C | CA5644188 | ABCC2 | c.4557A>C (p.Glu1519Asp) c.627A>C c.3861A>C (p.Glu1287Asp) | dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.99851550A>G | CA471136059 | ABCC2 | c.4557A>G (p.Glu1519=) c.627A>G c.3861A>G (p.Glu1287=) | |
10 | g.99851550A>T | CA378130749 | ABCC2 | c.4557A>T (p.Glu1519Asp) c.627A>T c.3861A>T (p.Glu1287Asp) | |
10 | g.99851551G>A | CA212872977 | ABCC2 | c.4558G>A (p.Glu1520Lys) c.628G>A c.3862G>A (p.Glu1288Lys) | dbSNP |
10 | g.99851551G>C | CA378130750 | ABCC2 | c.4558G>C (p.Glu1520Gln) c.628G>C c.3862G>C (p.Glu1288Gln) |