Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.186205151C=CA1519888877CYP4V2c.988-49C= (p.=)
n.223-49C=
n.5637C=
n.78-49C=
c.592-49C= (p.=)
4g.186205151C>TCA557054528CYP4V2c.988-49C>T (p.=)
n.223-49C>T
n.5637C>T
n.78-49C>T
c.592-49C>T (p.=)
gnomAD
4g.186205152A=CA1519888879CYP4V2c.988-48A= (p.=)
n.223-48A=
n.5638A=
n.78-48A=
c.592-48A= (p.=)
4g.186205152A>GCA557054529CYP4V2c.988-48A>G (p.=)
n.223-48A>G
n.5638A>G
n.78-48A>G
c.592-48A>G (p.=)
gnomAD
4g.186205154C=CA1519888881CYP4V2c.988-46C= (p.=)
n.223-46C=
n.5640C=
n.78-46C=
c.592-46C= (p.=)
4g.186205154C>TCA3162714CYP4V2c.988-46C>T (p.=)
n.223-46C>T
n.5640C>T
n.78-46C>T
c.592-46C>T (p.=)
dbSNP ExAC gnomAD
4g.186205155G>ACA3162715CYP4V2c.988-45G>A (p.=)
n.223-45G>A
n.5641G>A
n.78-45G>A
c.592-45G>A (p.=)
dbSNP ExAC gnomAD
4g.186205155G=CA1519888885CYP4V2c.988-45G= (p.=)
n.223-45G=
n.5641G=
n.78-45G=
c.592-45G= (p.=)
4g.186205155G>TCA1519888887CYP4V2c.988-45G>T (p.=)
n.223-45G>T
n.5641G>T
n.78-45G>T
c.592-45G>T (p.=)
4g.186205156C>ACA557054530CYP4V2c.988-44C>A (p.=)
n.223-44C>A
n.5642C>A
n.78-44C>A
c.592-44C>A (p.=)
gnomAD
4g.186205156C=CA1519888889CYP4V2c.988-44C= (p.=)
n.223-44C=
n.5642C=
n.78-44C=
c.592-44C= (p.=)
4g.186205159C=CA1519888890CYP4V2c.988-41C= (p.=)
n.223-41C=
n.5645C=
n.78-41C=
c.592-41C= (p.=)
4g.186205159C>GCA112131560CYP4V2c.988-41C>G (p.=)
n.223-41C>G
n.5645C>G
n.78-41C>G
c.592-41C>G (p.=)
dbSNP
4g.186205159C>TCA3162716CYP4V2c.988-41C>T (p.=)
n.223-41C>T
n.5645C>T
n.78-41C>T
c.592-41C>T (p.=)
dbSNP ExAC gnomAD
4g.186205160A=CA1519888893CYP4V2c.988-40A= (p.=)
n.223-40A=
n.5646A=
n.78-40A=
c.592-40A= (p.=)
4g.186205160A>GCA557054531CYP4V2c.988-40A>G (p.=)
n.223-40A>G
n.5646A>G
n.78-40A>G
c.592-40A>G (p.=)
gnomAD
4g.186205161T>CCA792325324CYP4V2c.988-39T>C (p.=)
n.223-39T>C
n.5647T>C
n.78-39T>C
c.592-39T>C (p.=)
4g.186205161T=CA1519888896CYP4V2c.988-39T= (p.=)
n.223-39T=
n.5647T=
n.78-39T=
c.592-39T= (p.=)
4g.186205163_186205165delinsACTCA1519888898CYP4V2c.988-37_988-35delinsACT (p.=)
n.223-37_223-35delinsACT
n.5649_5651delinsACT
n.78-37_78-35delinsACT
c.592-37_592-35delinsACT (p.=)
4g.186205166_186205167delCA3162717CYP4V2c.988-34_988-33del (p.=)
n.223-34_223-33del
n.5652_5653del
n.78-34_78-33del
c.592-34_592-33del (p.=)
dbSNP ExAC gnomAD
4g.186205167_186205168delinsTGCA1519888899CYP4V2c.988-33_988-32delinsTG (p.=)
n.223-33_223-32delinsTG
n.5653_5654delinsTG
n.78-33_78-32delinsTG
c.592-33_592-32delinsTG (p.=)
4g.186205168delCA3162718CYP4V2c.988-32del (p.=)
n.223-32del
n.5654del
n.78-32del
c.592-32del (p.=)
dbSNP ExAC gnomAD
4g.186205168G>ACA1519888902CYP4V2c.988-32G>A (p.=)
n.223-32G>A
n.5654G>A
n.78-32G>A
c.592-32G>A (p.=)
4g.186205168G=CA1519888901CYP4V2c.988-32G= (p.=)
n.223-32G=
n.5654G=
n.78-32G=
c.592-32G= (p.=)
4g.186205169delCA358949187CYP4V2c.988-31del (p.=)
n.223-31del
n.5655del
n.78-31del
c.592-31del (p.=)
4g.186205170T>CCA3162719CYP4V2c.988-30T>C (p.=)
n.223-30T>C
n.5656T>C
n.78-30T>C
c.592-30T>C (p.=)
dbSNP ExAC gnomAD
4g.186205170T=CA1519888904CYP4V2c.988-30T= (p.=)
n.223-30T=
n.5656T=
n.78-30T=
c.592-30T= (p.=)
4g.186205173T>CCA557054532CYP4V2c.988-27T>C (p.=)
n.223-27T>C
n.5659T>C
n.78-27T>C
c.592-27T>C (p.=)
gnomAD
4g.186205173T=CA1519888906CYP4V2c.988-27T= (p.=)
n.223-27T=
n.5659T=
n.78-27T=
c.592-27T= (p.=)
4g.186205179T>GCA1519888909CYP4V2c.988-21T>G (p.=)
n.223-21T>G
n.5665T>G
n.78-21T>G
c.592-21T>G (p.=)
4g.186205179T=CA1519888908CYP4V2c.988-21T= (p.=)
n.223-21T=
n.5665T=
n.78-21T=
c.592-21T= (p.=)
4g.186205180A=CA1519888911CYP4V2c.988-20A= (p.=)
n.223-20A=
n.5666A=
n.78-20A=
c.592-20A= (p.=)
4g.186205180A>GCA3162720CYP4V2c.988-20A>G (p.=)
n.223-20A>G
n.5666A>G
n.78-20A>G
c.592-20A>G (p.=)
ClinVar dbSNP ExAC gnomAD
4g.186205181T>CCA557054533CYP4V2c.988-19T>C (p.=)
n.223-19T>C
n.5667T>C
n.78-19T>C
c.592-19T>C (p.=)
gnomAD
4g.186205181T=CA1519888912CYP4V2c.988-19T= (p.=)
n.223-19T=
n.5667T=
n.78-19T=
c.592-19T= (p.=)
4g.186205187T>ACA112131570CYP4V2c.988-13T>A (p.=)
n.223-13T>A
n.5673T>A
n.78-13T>A
c.592-13T>A (p.=)
dbSNP
4g.186205187T=CA1519888914CYP4V2c.988-13T= (p.=)
n.223-13T=
n.5673T=
n.78-13T=
c.592-13T= (p.=)
4g.186205188C=CA1519888916CYP4V2c.988-12C= (p.=)
n.223-12C=
n.5674C=
n.78-12C=
c.592-12C= (p.=)
4g.186205188C>TCA3162721CYP4V2c.988-12C>T (p.=)
n.223-12C>T
n.5674C>T
n.78-12C>T
c.592-12C>T (p.=)
dbSNP ExAC gnomAD
4g.186205191C=CA1519888918CYP4V2c.988-9C= (p.=)
n.223-9C=
n.5677C=
n.78-9C=
c.592-9C= (p.=)
4g.186205191C>TCA557054534CYP4V2c.988-9C>T (p.=)
n.223-9C>T
n.5677C>T
n.78-9C>T
c.592-9C>T (p.=)
ClinVar gnomAD
4g.186205196G=CA1519888920CYP4V2c.988-4G= (p.=)
n.223-4G=
n.5682G=
n.78-4G=
c.592-4G= (p.=)
4g.186205196G>TCA557054535CYP4V2c.988-4G>T (p.=)
n.223-4G>T
n.5682G>T
n.78-4G>T
c.592-4G>T (p.=)
gnomAD
4g.186205197T>CCA1519888922CYP4V2c.988-3T>C (p.=)
n.223-3T>C
n.5683T>C
n.78-3T>C
c.592-3T>C (p.=)
4g.186205197T=CA1519888921CYP4V2c.988-3T= (p.=)
n.223-3T=
n.5683T=
n.78-3T=
c.592-3T= (p.=)
4g.186205198A=CA1519888926CYP4V2c.988-2A= (p.=)
n.223-2A=
n.5684A=
n.78-2A=
c.592-2A= (p.=)
4g.186205198A>CCA358949188CYP4V2c.988-2A>C (p.=)
n.223-2A>C
n.5684A>C
n.78-2A>C
c.592-2A>C (p.=)
4g.186205198A>GCA358949189CYP4V2c.988-2A>G (p.=)
n.223-2A>G
n.5684A>G
n.78-2A>G
c.592-2A>G (p.=)
4g.186205198A>TCA358949190CYP4V2c.988-2A>T (p.=)
n.223-2A>T
n.5684A>T
n.78-2A>T
c.592-2A>T (p.=)
4g.186205198_186205199delinsAGCA1519888928CYP4V2c.988-2_988-1delinsAG (p.=)
n.223-2_223-1delinsAG
n.5684_5685delinsAG
n.78-2_78-1delinsAG
c.592-2_592-1delinsAG (p.=)

Number of alleles fetched