Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.1610446_1613897del | CA891843163 | FOXC1 | c.1_*1790del (n.[c.1_*1790del;Met1=]) c.1_3452del (n.[c.1_3452del;Met1=]) | ClinVar |
6 | g.1610685_1610729del | CA2695205854 | FOXC1 | c.240_284del (p.Tyr81_Pro95del) | |
6 | g.1610700_1610701delinsTT | CA2695205857 | FOXC1 | c.255_256delinsTT (p.Leu86Phe) | |
6 | g.1610701_1610712del | CA2573140134 | FOXC1 | c.256_267del (p.Leu86_Met89del) | ClinVar dbSNP |
6 | g.1610701C>A | CA362558414 | FOXC1 | c.256C>A (p.Leu86Ile) | |
6 | g.1610701C= | CA1605822456 | FOXC1 | c.256C= (p.Leu86=) | |
6 | g.1610701C>G | CA362558415 | FOXC1 | c.256C>G (p.Leu86Val) | |
6 | g.1610701C>T | CA10588416 | FOXC1 | c.256C>T (p.Leu86Phe) | ClinVar dbSNP |
6 | g.1610702T>A | CA362558417 | FOXC1 | c.257T>A (p.Leu86His) | |
6 | g.1610702T>C | CA362558418 | FOXC1 | c.257T>C (p.Leu86Pro) | |
6 | g.1610702T>G | CA362558416 | FOXC1 | c.257T>G (p.Leu86Arg) | ClinVar |
6 | g.1610702_1610703insTA | CA645541563 | FOXC1 | c.257_258insTA (p.Ile87ThrfsTer16) | COSMIC |
6 | g.1610703C>A | CA448393251 | FOXC1 | c.258C>A (p.Leu86=) | COSMIC |
6 | g.1610703C= | CA1605822457 | FOXC1 | c.258C= (p.Leu86=) | |
6 | g.1610703C>G | CA448393252 | FOXC1 | c.258C>G (p.Leu86=) | |
6 | g.1610703C>T | CA448393253 | FOXC1 | c.258C>T (p.Leu86=) | dbSNP gnomAD v4 |
6 | g.1610704A>C | CA362558419 | FOXC1 | c.259A>C (p.Ile87Leu) | |
6 | g.1610704A>G | CA362558421 | FOXC1 | c.259A>G (p.Ile87Val) | gnomAD v4 |
6 | g.1610704A>T | CA362558420 | FOXC1 | c.259A>T (p.Ile87Phe) | |
6 | g.1610705T>A | CA362558422 | FOXC1 | c.260T>A (p.Ile87Asn) | |
6 | g.1610705T>C | CA362558424 | FOXC1 | c.260T>C (p.Ile87Thr) | |
6 | g.1610705T>G | CA362558423 | FOXC1 | c.260T>G (p.Ile87Ser) | |
6 | g.1610706C>A | CA448393259 | FOXC1 | c.261C>A (p.Ile87=) | |
6 | g.1610706C= | CA1605822458 | FOXC1 | c.261C= (p.Ile87=) | |
6 | g.1610706C>G | CA119641 | FOXC1 | c.261C>G (p.Ile87Met) | ClinVar dbSNP |
6 | g.1610706C>T | CA448393258 | FOXC1 | c.261C>T (p.Ile87=) | ClinVar gnomAD v4 |
6 | g.1610707A= | CA1605822459 | FOXC1 | c.262A= (p.Thr88=) | |
6 | g.1610707A>C | CA362558425 | FOXC1 | c.262A>C (p.Thr88Pro) | ClinVar dbSNP |
6 | g.1610707A>G | CA362558426 | FOXC1 | c.262A>G (p.Thr88Ala) | |
6 | g.1610707A>T | CA362558427 | FOXC1 | c.262A>T (p.Thr88Ser) | |
6 | g.1610708C>A | CA362558428 | FOXC1 | c.263C>A (p.Thr88Asn) | |
6 | g.1610708C= | CA1605822460 | FOXC1 | c.263C= (p.Thr88=) | |
6 | g.1610708C>G | CA362558429 | FOXC1 | c.263C>G (p.Thr88Ser) | |
6 | g.1610708C>T | CA234027 | FOXC1 | c.263C>T (p.Thr88Ile) | ClinVar dbSNP |
6 | g.1610709dup | CA2497029025 | FOXC1 | c.264dup (p.Met89HisfsTer?) | |
6 | g.1610709C>A | CA448393263 | FOXC1 | c.264C>A (p.Thr88=) | |
6 | g.1610709C= | CA1605822461 | FOXC1 | c.264C= (p.Thr88=) | |
6 | g.1610709C>G | CA448393265 | FOXC1 | c.264C>G (p.Thr88=) | gnomAD v4 |
6 | g.1610709C>T | CA448393267 | FOXC1 | c.264C>T (p.Thr88=) | ClinVar dbSNP gnomAD v4 |
6 | g.1610710A>C | CA362558430 | FOXC1 | c.265A>C (p.Met89Leu) | |
6 | g.1610710A>G | CA362558431 | FOXC1 | c.265A>G (p.Met89Val) | gnomAD v4 |
6 | g.1610710A>T | CA362558432 | FOXC1 | c.265A>T (p.Met89Leu) | |
6 | g.1610711T>A | CA362558435 | FOXC1 | c.266T>A (p.Met89Lys) | |
6 | g.1610711T>C | CA362558433 | FOXC1 | c.266T>C (p.Met89Thr) | |
6 | g.1610711T>G | CA362558434 | FOXC1 | c.266T>G (p.Met89Arg) | |
6 | g.1610712G>A | CA362558436 | FOXC1 | c.267G>A (p.Met89Ile) | gnomAD v4 |
6 | g.1610712G>C | CA362558437 | FOXC1 | c.267G>C (p.Met89Ile) | |
6 | g.1610712G>T | CA362558438 | FOXC1 | c.267G>T (p.Met89Ile) | |
6 | g.1610713G>A | CA16044261 | FOXC1 | c.268G>A (p.Ala90Thr) | ClinVar dbSNP |
6 | g.1610713G>C | CA362558439 | FOXC1 | c.268G>C (p.Ala90Pro) |