Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.215404591C>A | CA204749 | FN1 | c.3051G>T (p.Trp1017Cys) | ClinVar dbSNP |
2 | g.215404591C= | CA1327359808 | FN1 | c.3051G= (p.Trp1017=) | |
2 | g.215404591C>G | CA350489456 | FN1 | c.3051G>C (p.Trp1017Cys) | |
2 | g.215404591C>T | CA350489457 | FN1 | c.3051G>A (p.Trp1017Ter) | |
2 | g.215404592C>A | CA350489458 | FN1 | c.3050G>T (p.Trp1017Leu) | |
2 | g.215404592C>G | CA350489459 | FN1 | c.3050G>C (p.Trp1017Ser) | |
2 | g.215404592C>T | CA350489460 | FN1 | c.3050G>A (p.Trp1017Ter) | COSMIC COSMIC |
2 | g.215404593A>C | CA350489461 | FN1 | c.3049T>G (p.Trp1017Gly) | |
2 | g.215404593A>G | CA350489463 | FN1 | c.3049T>C (p.Trp1017Arg) | |
2 | g.215404593A>T | CA350489462 | FN1 | c.3049T>A (p.Trp1017Arg) | |
2 | g.215404594T>A | CA350489464 | FN1 | c.3048A>T (p.Arg1016Ser) | |
2 | g.215404594T>C | CA431158083 | FN1 | c.3048A>G (p.Arg1016=) | gnomAD v4 |
2 | g.215404594T>G | CA350489465 | FN1 | c.3048A>C (p.Arg1016Ser) | |
2 | g.215404595C>A | CA350489466 | FN1 | c.3047G>T (p.Arg1016Ile) | |
2 | g.215404595C= | CA1327359809 | FN1 | c.3047G= (p.Arg1016=) | |
2 | g.215404595C>G | CA2094808 | FN1 | c.3047G>C (p.Arg1016Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.215404595C>T | CA350489467 | FN1 | c.3047G>A (p.Arg1016Lys) | |
2 | g.215404596T>A | CA350489469 | FN1 | c.3046A>T (p.Arg1016Ter) | |
2 | g.215404596T>C | CA350489468 | FN1 | c.3046A>G (p.Arg1016Gly) | |
2 | g.215404596T>G | CA431158085 | FN1 | c.3046A>C (p.Arg1016=) | |
2 | g.215404597C>A | CA431158088 | FN1 | c.3045G>T (p.Val1015=) | |
2 | g.215404597C>G | CA431158089 | FN1 | c.3045G>C (p.Val1015=) | |
2 | g.215404597C>T | CA431158090 | FN1 | c.3045G>A (p.Val1015=) | |
2 | g.215404598A>C | CA350489470 | FN1 | c.3044T>G (p.Val1015Gly) | |
2 | g.215404598A>G | CA350489472 | FN1 | c.3044T>C (p.Val1015Ala) | |
2 | g.215404598A>T | CA350489471 | FN1 | c.3044T>A (p.Val1015Glu) | |
2 | g.215404599C>A | CA350489473 | FN1 | c.3043G>T (p.Val1015Leu) | gnomAD v4 |
2 | g.215404599C>G | CA350489475 | FN1 | c.3043G>C (p.Val1015Leu) | |
2 | g.215404599C>T | CA350489474 | FN1 | c.3043G>A (p.Val1015Met) | |
2 | g.215404600C>A | CA431158091 | FN1 | c.3042G>T (p.Leu1014=) | |
2 | g.215404600C>G | CA431158092 | FN1 | c.3042G>C (p.Leu1014=) | |
2 | g.215404600C>T | CA431158093 | FN1 | c.3042G>A (p.Leu1014=) | |
2 | g.215404601A>C | CA350489476 | FN1 | c.3041T>G (p.Leu1014Arg) | |
2 | g.215404601A>G | CA350489477 | FN1 | c.3041T>C (p.Leu1014Pro) | |
2 | g.215404601A>T | CA350489478 | FN1 | c.3041T>A (p.Leu1014Gln) | |
2 | g.215404602G>A | CA431158095 | FN1 | c.3040C>T (p.Leu1014=) | dbSNP |
2 | g.215404602G>C | CA350489479 | FN1 | c.3040C>G (p.Leu1014Val) | |
2 | g.215404602G= | CA1327359810 | FN1 | c.3040C= (p.Leu1014=) | |
2 | g.215404602G>T | CA350489480 | FN1 | c.3040C>A (p.Leu1014Met) | |
2 | g.215404603G>A | CA431158096 | FN1 | c.3039C>T (p.Val1013=) | |
2 | g.215404603G>C | CA431158097 | FN1 | c.3039C>G (p.Val1013=) | |
2 | g.215404603G>T | CA431158098 | FN1 | c.3039C>A (p.Val1013=) | |
2 | g.215404604A>C | CA350489483 | FN1 | c.3038T>G (p.Val1013Gly) | |
2 | g.215404604A>G | CA350489482 | FN1 | c.3038T>C (p.Val1013Ala) | |
2 | g.215404604A>T | CA350489481 | FN1 | c.3038T>A (p.Val1013Asp) | |
2 | g.215404605C>A | CA350489484 | FN1 | c.3037G>T (p.Val1013Phe) | |
2 | g.215404605C>G | CA350489485 | FN1 | c.3037G>C (p.Val1013Leu) | |
2 | g.215404605C>T | CA350489486 | FN1 | c.3037G>A (p.Val1013Ile) | |
2 | g.215404606A>C | CA431158099 | FN1 | c.3036T>G (p.Thr1012=) | |
2 | g.215404606A>G | CA431158101 | FN1 | c.3036T>C (p.Thr1012=) |