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.1610832C>A | CA362558708 | FOXC1 | c.387C>A (p.Asn129Lys) | ClinVar dbSNP |
6 | g.1610832C= | CA1605822528 | FOXC1 | c.387C= (p.Asn129=) | |
6 | g.1610832C>G | CA362558707 | FOXC1 | c.387C>G (p.Asn129Lys) | |
6 | g.1610832C>T | CA3614752 | FOXC1 | c.387C>T (p.Asn129=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.1610833C>A | CA362558709 | FOXC1 | c.388C>A (p.Leu130Ile) | |
6 | g.1610833C= | CA1605822529 | FOXC1 | c.388C= (p.Leu130=) | |
6 | g.1610833C>G | CA362558710 | FOXC1 | c.388C>G (p.Leu130Val) | |
6 | g.1610833C>T | CA119643 | FOXC1 | c.388C>T (p.Leu130Phe) | ClinVar dbSNP |
6 | g.1610834_1610837del | CA2739272831 | FOXC1 | c.389_392del (p.Leu130ArgfsTer?) | ClinVar |
6 | g.1610834T>A | CA362558711 | FOXC1 | c.389T>A (p.Leu130His) | |
6 | g.1610834T>C | CA362558712 | FOXC1 | c.389T>C (p.Leu130Pro) | COSMIC |
6 | g.1610834T>G | CA362558713 | FOXC1 | c.389T>G (p.Leu130Arg) | |
6 | g.1610835C>A | CA448393580 | FOXC1 | c.390C>A (p.Leu130=) | |
6 | g.1610835C= | CA1605822530 | FOXC1 | c.390C= (p.Leu130=) | |
6 | g.1610835C>G | CA448393583 | FOXC1 | c.390C>G (p.Leu130=) | dbSNP gnomAD v4 |
6 | g.1610835C>T | CA448393581 | FOXC1 | c.390C>T (p.Leu130=) | |
6 | g.1610836T>A | CA362558714 | FOXC1 | c.391T>A (p.Ser131Thr) | |
6 | g.1610836T>C | CA362558715 | FOXC1 | c.391T>C (p.Ser131Pro) | |
6 | g.1610836T>G | CA362558716 | FOXC1 | c.391T>G (p.Ser131Ala) | |
6 | g.1610837C>A | CA362558717 | FOXC1 | c.392C>A (p.Ser131Ter) | ClinVar |
6 | g.1610837C= | CA1605822531 | FOXC1 | c.392C= (p.Ser131=) | |
6 | g.1610837C>G | CA362558718 | FOXC1 | c.392C>G (p.Ser131Trp) | ClinVar dbSNP |
6 | g.1610837C>T | CA119632 | FOXC1 | c.392C>T (p.Ser131Leu) | ClinVar dbSNP |
6 | g.1610838G>A | CA448393585 | FOXC1 | c.393G>A (p.Ser131=) | gnomAD v4 COSMIC |
6 | g.1610838G>C | CA448393586 | FOXC1 | c.393G>C (p.Ser131=) | gnomAD v4 |
6 | g.1610838G>T | CA448393587 | FOXC1 | c.393G>T (p.Ser131=) | |
6 | g.1610839C>A | CA362558721 | FOXC1 | c.394C>A (p.Leu132Ile) | gnomAD v4 |
6 | g.1610839C>G | CA362558720 | FOXC1 | c.394C>G (p.Leu132Val) | |
6 | g.1610839C>T | CA362558719 | FOXC1 | c.394C>T (p.Leu132Phe) | |
6 | g.1610840T>A | CA362558722 | FOXC1 | c.395T>A (p.Leu132His) | |
6 | g.1610840T>C | CA362558723 | FOXC1 | c.395T>C (p.Leu132Pro) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.1610840T>G | CA362558724 | FOXC1 | c.395T>G (p.Leu132Arg) | |
6 | g.1610840T= | CA1605822532 | FOXC1 | c.395T= (p.Leu132=) | |
6 | g.1610841C>A | CA448393589 | FOXC1 | c.396C>A (p.Leu132=) | |
6 | g.1610841C= | CA1605822533 | FOXC1 | c.396C= (p.Leu132=) | |
6 | g.1610841C>G | CA448393590 | FOXC1 | c.396C>G (p.Leu132=) | COSMIC |
6 | g.1610841C>T | CA448393591 | FOXC1 | c.396C>T (p.Leu132=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
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) |