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.1610701_1610712del | CA2573140134 | FOXC1 | c.256_267del (p.Leu86_Met89del) | ClinVar dbSNP |
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) | |
6 | g.1610713G= | CA1605822462 | FOXC1 | c.268G= (p.Ala90=) | |
6 | g.1610713G>T | CA362558440 | FOXC1 | c.268G>T (p.Ala90Ser) | gnomAD v4 |
6 | g.1610714C>A | CA16044262 | FOXC1 | c.269C>A (p.Ala90Asp) | ClinVar dbSNP |
6 | g.1610714C= | CA1605822463 | FOXC1 | c.269C= (p.Ala90=) | |
6 | g.1610714C>G | CA362558441 | FOXC1 | c.269C>G (p.Ala90Gly) | |
6 | g.1610714C>T | CA362558442 | FOXC1 | c.269C>T (p.Ala90Val) | ClinVar |
6 | g.1610715C>A | CA448393275 | FOXC1 | c.270C>A (p.Ala90=) | |
6 | g.1610715C= | CA1605822464 | FOXC1 | c.270C= (p.Ala90=) | |
6 | g.1610715C>G | CA3614728 | FOXC1 | c.270C>G (p.Ala90=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.1610715C>T | CA448393277 | FOXC1 | c.270C>T (p.Ala90=) | dbSNP gnomAD v2 gnomAD v4 |
6 | g.1610716A>C | CA362558444 | FOXC1 | c.271A>C (p.Ile91Leu) | |
6 | g.1610716A>G | CA362558445 | FOXC1 | c.271A>G (p.Ile91Val) | |
6 | g.1610716A>T | CA362558443 | FOXC1 | c.271A>T (p.Ile91Phe) |