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.1610832C>ACA362558708FOXC1c.387C>A (p.Asn129Lys)
ClinVar dbSNP
6g.1610832C=CA1605822528FOXC1c.387C= (p.Asn129=)
6g.1610832C>GCA362558707FOXC1c.387C>G (p.Asn129Lys)
6g.1610832C>TCA3614752FOXC1c.387C>T (p.Asn129=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.1610833C>ACA362558709FOXC1c.388C>A (p.Leu130Ile)
6g.1610833C=CA1605822529FOXC1c.388C= (p.Leu130=)
6g.1610833C>GCA362558710FOXC1c.388C>G (p.Leu130Val)
6g.1610833C>TCA119643FOXC1c.388C>T (p.Leu130Phe)
ClinVar dbSNP
6g.1610834_1610837delCA2739272831FOXC1c.389_392del (p.Leu130ArgfsTer?)
ClinVar
6g.1610834T>ACA362558711FOXC1c.389T>A (p.Leu130His)
6g.1610834T>CCA362558712FOXC1c.389T>C (p.Leu130Pro)
COSMIC
6g.1610834T>GCA362558713FOXC1c.389T>G (p.Leu130Arg)
6g.1610835C>ACA448393580FOXC1c.390C>A (p.Leu130=)
6g.1610835C=CA1605822530FOXC1c.390C= (p.Leu130=)
6g.1610835C>GCA448393583FOXC1c.390C>G (p.Leu130=)
dbSNP gnomAD v4
6g.1610835C>TCA448393581FOXC1c.390C>T (p.Leu130=)
6g.1610836T>ACA362558714FOXC1c.391T>A (p.Ser131Thr)
6g.1610836T>CCA362558715FOXC1c.391T>C (p.Ser131Pro)
6g.1610836T>GCA362558716FOXC1c.391T>G (p.Ser131Ala)
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)

Number of alleles fetched