Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.1610446_1613897delCA891843163FOXC1c.1_*1790del (n.[c.1_*1790del;Met1=])
c.1_3452del (n.[c.1_3452del;Met1=])
ClinVar
6g.1610834_1610837delCA2739272831FOXC1c.389_392del (p.Leu130ArgfsTer?)
ClinVar
6g.1610837C>ACA362558717FOXC1c.392C>A (p.Ser131Ter)
ClinVar
6g.1610837C=CA1605822531FOXC1c.392C= (p.Ser131=)
6g.1610837C>GCA362558718FOXC1c.392C>G (p.Ser131Trp)
ClinVar dbSNP
6g.1610837C>TCA119632FOXC1c.392C>T (p.Ser131Leu)
ClinVar dbSNP
6g.1610838G>ACA448393585FOXC1c.393G>A (p.Ser131=)
gnomAD v4 COSMIC
6g.1610838G>CCA448393586FOXC1c.393G>C (p.Ser131=)
gnomAD v4
6g.1610838G>TCA448393587FOXC1c.393G>T (p.Ser131=)
6g.1610839C>ACA362558721FOXC1c.394C>A (p.Leu132Ile)
gnomAD v4
6g.1610839C>GCA362558720FOXC1c.394C>G (p.Leu132Val)
6g.1610839C>TCA362558719FOXC1c.394C>T (p.Leu132Phe)
6g.1610840T>ACA362558722FOXC1c.395T>A (p.Leu132His)
6g.1610840T>CCA362558723FOXC1c.395T>C (p.Leu132Pro)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.1610840T>GCA362558724FOXC1c.395T>G (p.Leu132Arg)
6g.1610840T=CA1605822532FOXC1c.395T= (p.Leu132=)
6g.1610841C>ACA448393589FOXC1c.396C>A (p.Leu132=)
6g.1610841C=CA1605822533FOXC1c.396C= (p.Leu132=)
6g.1610841C>GCA448393590FOXC1c.396C>G (p.Leu132=)
COSMIC
6g.1610841C>TCA448393591FOXC1c.396C>T (p.Leu132=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.1610842A>CCA362558725FOXC1c.397A>C (p.Asn133His)
6g.1610842A>GCA362558726FOXC1c.397A>G (p.Asn133Asp)
6g.1610842A>TCA362558727FOXC1c.397A>T (p.Asn133Tyr)
6g.1610843_1610846delCA2573140135FOXC1c.398_401del (p.Asn133SerfsTer?)
ClinVar dbSNP
6g.1610843A>CCA362558728FOXC1c.398A>C (p.Asn133Thr)
6g.1610843A>GCA362558729FOXC1c.398A>G (p.Asn133Ser)
6g.1610843A>TCA362558730FOXC1c.398A>T (p.Asn133Ile)
6g.1610844C>ACA362558731FOXC1c.399C>A (p.Asn133Lys)
6g.1610844C=CA1605822534FOXC1c.399C= (p.Asn133=)
6g.1610844C>GCA362558732FOXC1c.399C>G (p.Asn133Lys)
ClinVar dbSNP
6g.1610844C>TCA133389929FOXC1c.399C>T (p.Asn133=)
dbSNP gnomAD v4
6g.1610845G>ACA362558734FOXC1c.400G>A (p.Glu134Lys)
6g.1610845G>CCA362558735FOXC1c.400G>C (p.Glu134Gln)
6g.1610845G>TCA362558733FOXC1c.400G>T (p.Glu134Ter)
6g.1610846A>CCA362558736FOXC1c.401A>C (p.Glu134Ala)
6g.1610846A>GCA362558737FOXC1c.401A>G (p.Glu134Gly)
6g.1610846A>TCA362558738FOXC1c.401A>T (p.Glu134Val)
6g.1610847G>ACA133389931FOXC1c.402G>A (p.Glu134=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.1610847G>CCA362558739FOXC1c.402G>C (p.Glu134Asp)
COSMIC
6g.1610847G=CA1605822535FOXC1c.402G= (p.Glu134=)
6g.1610847G>TCA362558740FOXC1c.402G>T (p.Glu134Asp)
6g.1610851_1610863delCA2580617996FOXC1c.406_418del (p.Phe136ArgfsTer?)
ClinVar
6g.1610848T>ACA362558743FOXC1c.403T>A (p.Cys135Ser)
ClinVar
6g.1610848T>CCA362558741FOXC1c.403T>C (p.Cys135Arg)
COSMIC
6g.1610848T>GCA362558742FOXC1c.403T>G (p.Cys135Gly)
6g.1610849G>ACA362558744FOXC1c.404G>A (p.Cys135Tyr)
ClinVar COSMIC
6g.1610849G>CCA362558745FOXC1c.404G>C (p.Cys135Ser)
6g.1610849G>TCA362558746FOXC1c.404G>T (p.Cys135Phe)
6g.1610850C>ACA362558747FOXC1c.405C>A (p.Cys135Ter)
ClinVar dbSNP
6g.1610850C=CA1605822536FOXC1c.405C= (p.Cys135=)

Number of alleles fetched