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.1610842A>C | CA362558725 | FOXC1 | c.397A>C (p.Asn133His) | |
6 | g.1610842A>G | CA362558726 | FOXC1 | c.397A>G (p.Asn133Asp) | |
6 | g.1610842A>T | CA362558727 | FOXC1 | c.397A>T (p.Asn133Tyr) | |
6 | g.1610843_1610846del | CA2573140135 | FOXC1 | c.398_401del (p.Asn133SerfsTer?) | ClinVar dbSNP |
6 | g.1610843A>C | CA362558728 | FOXC1 | c.398A>C (p.Asn133Thr) | |
6 | g.1610843A>G | CA362558729 | FOXC1 | c.398A>G (p.Asn133Ser) | |
6 | g.1610843A>T | CA362558730 | FOXC1 | c.398A>T (p.Asn133Ile) | |
6 | g.1610844C>A | CA362558731 | FOXC1 | c.399C>A (p.Asn133Lys) | |
6 | g.1610844C= | CA1605822534 | FOXC1 | c.399C= (p.Asn133=) | |
6 | g.1610844C>G | CA362558732 | FOXC1 | c.399C>G (p.Asn133Lys) | ClinVar dbSNP |
6 | g.1610844C>T | CA133389929 | FOXC1 | c.399C>T (p.Asn133=) | dbSNP gnomAD v4 |
6 | g.1610845G>A | CA362558734 | FOXC1 | c.400G>A (p.Glu134Lys) | |
6 | g.1610845G>C | CA362558735 | FOXC1 | c.400G>C (p.Glu134Gln) | |
6 | g.1610845G>T | CA362558733 | FOXC1 | c.400G>T (p.Glu134Ter) | |
6 | g.1610846A>C | CA362558736 | FOXC1 | c.401A>C (p.Glu134Ala) | |
6 | g.1610846A>G | CA362558737 | FOXC1 | c.401A>G (p.Glu134Gly) | |
6 | g.1610846A>T | CA362558738 | FOXC1 | c.401A>T (p.Glu134Val) | |
6 | g.1610847G>A | CA133389931 | FOXC1 | c.402G>A (p.Glu134=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.1610847G>C | CA362558739 | FOXC1 | c.402G>C (p.Glu134Asp) | COSMIC |
6 | g.1610847G= | CA1605822535 | FOXC1 | c.402G= (p.Glu134=) | |
6 | g.1610847G>T | CA362558740 | FOXC1 | c.402G>T (p.Glu134Asp) | |
6 | g.1610851_1610863del | CA2580617996 | FOXC1 | c.406_418del (p.Phe136ArgfsTer?) | ClinVar |
6 | g.1610848T>A | CA362558743 | FOXC1 | c.403T>A (p.Cys135Ser) | ClinVar |
6 | g.1610848T>C | CA362558741 | FOXC1 | c.403T>C (p.Cys135Arg) | COSMIC |
6 | g.1610848T>G | CA362558742 | FOXC1 | c.403T>G (p.Cys135Gly) | |
6 | g.1610849G>A | CA362558744 | FOXC1 | c.404G>A (p.Cys135Tyr) | ClinVar COSMIC |
6 | g.1610849G>C | CA362558745 | FOXC1 | c.404G>C (p.Cys135Ser) | |
6 | g.1610849G>T | CA362558746 | FOXC1 | c.404G>T (p.Cys135Phe) | |
6 | g.1610850C>A | CA362558747 | FOXC1 | c.405C>A (p.Cys135Ter) | ClinVar dbSNP |
6 | g.1610850C= | CA1605822536 | FOXC1 | c.405C= (p.Cys135=) | |
6 | g.1610850C>G | CA362558748 | FOXC1 | c.405C>G (p.Cys135Trp) | |
6 | g.1610850C>T | CA180044 | FOXC1 | c.405C>T (p.Cys135=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.1610851T>A | CA362558750 | FOXC1 | c.406T>A (p.Phe136Ile) | |
6 | g.1610851T>C | CA362558751 | FOXC1 | c.406T>C (p.Phe136Leu) | |
6 | g.1610851T>G | CA362558749 | FOXC1 | c.406T>G (p.Phe136Val) | |
6 | g.1610851_1610854delinsTTCG | CA1605822537 | FOXC1 | c.406_409delinsTTCG (p.Phe136=) | |
6 | g.1610852T>A | CA362558754 | FOXC1 | c.407T>A (p.Phe136Tyr) | |
6 | g.1610852T>C | CA362558752 | FOXC1 | c.407T>C (p.Phe136Ser) | ClinVar |
6 | g.1610852T>G | CA362558753 | FOXC1 | c.407T>G (p.Phe136Cys) | |
6 | g.1610854_1610856del | CA658683436 | FOXC1 | c.409_411del (p.Val137del) | ClinVar dbSNP |
6 | g.1610853C>A | CA362558755 | FOXC1 | c.408C>A (p.Phe136Leu) | |
6 | g.1610853C>G | CA362558756 | FOXC1 | c.408C>G (p.Phe136Leu) | |
6 | g.1610853C>T | CA448393604 | FOXC1 | c.408C>T (p.Phe136=) | gnomAD v4 |
6 | g.1610853_1610854insA | CA2769751901 | FOXC1 | c.408_409insA (p.Val137SerfsTer?) | |
6 | g.1610853_1610854insACA | CA2769751902 | FOXC1 | c.408_409insACA (p.Phe136_Val137insThr) | |
6 | g.1610853_1610854insTGTG | CA645541564 | FOXC1 | c.408_409insTGTG (p.Val137CysfsTer?) | COSMIC |
6 | g.1610854G>A | CA3614753 | FOXC1 | c.409G>A (p.Val137Ile) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.1610854G>C | CA3614754 | FOXC1 | c.409G>C (p.Val137Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.1610854G= | CA1605822538 | FOXC1 | c.409G= (p.Val137=) |