Chr Mutation (hg38) CAid Gene Transcript Linkouts
22g.42693330G>ACA515072369A4GALT,CYB5R3c.-49+27467C>T (n.-49+27467C>T)
c.622C>T (p.Leu208=)
22g.42693330G>CCA411811944A4GALT,CYB5R3c.-49+27467C>G (n.-49+27467C>G)
c.622C>G (p.Leu208Val)
22g.42693330G>TCA411811942A4GALT,CYB5R3c.-49+27467C>A (n.-49+27467C>A)
c.622C>A (p.Leu208Met)
22g.42693331C>ACA515072374A4GALT,CYB5R3c.-49+27466G>T (n.-49+27466G>T)
c.621G>T (p.Val207=)
22g.42693331C>GCA515072376A4GALT,CYB5R3c.-49+27466G>C (n.-49+27466G>C)
c.621G>C (p.Val207=)
22g.42693331C>TCA515072378A4GALT,CYB5R3c.-49+27466G>A (n.-49+27466G>A)
c.621G>A (p.Val207=)
22g.42693332A=CA2406870243A4GALT,CYB5R3c.-49+27465T= (n.-49+27465T=)
c.620T= (p.Val207=)
22g.42693332A>CCA10270255A4GALT,CYB5R3c.-49+27465T>G (n.-49+27465T>G)
c.620T>G (p.Val207Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
22g.42693332A>GCA411811947A4GALT,CYB5R3c.-49+27465T>C (n.-49+27465T>C)
c.620T>C (p.Val207Ala)
22g.42693332A>TCA411811945A4GALT,CYB5R3c.-49+27465T>A (n.-49+27465T>A)
c.620T>A (p.Val207Glu)
22g.42693333C>ACA411811949A4GALT,CYB5R3c.-49+27464G>T (n.-49+27464G>T)
c.619G>T (p.Val207Leu)
22g.42693333C=CA2406870244A4GALT,CYB5R3c.-49+27464G= (n.-49+27464G=)
c.619G= (p.Val207=)
22g.42693333C>GCA411811951A4GALT,CYB5R3c.-49+27464G>C (n.-49+27464G>C)
c.619G>C (p.Val207Leu)
22g.42693333C>TCA10270256A4GALT,CYB5R3c.-49+27464G>A (n.-49+27464G>A)
c.619G>A (p.Val207Met)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
22g.42693334G>ACA10270257A4GALT,CYB5R3c.-49+27463C>T (n.-49+27463C>T)
c.618C>T (p.Asn206=)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
22g.42693334G>CCA411811956A4GALT,CYB5R3c.-49+27463C>G (n.-49+27463C>G)
c.618C>G (p.Asn206Lys)
22g.42693334G=CA2406870245A4GALT,CYB5R3c.-49+27463C= (n.-49+27463C=)
c.618C= (p.Asn206=)
22g.42693334G>TCA411811958A4GALT,CYB5R3c.-49+27463C>A (n.-49+27463C>A)
c.618C>A (p.Asn206Lys)
22g.42693335T>ACA411811960A4GALT,CYB5R3c.-49+27462A>T (n.-49+27462A>T)
c.617A>T (p.Asn206Ile)
22g.42693335T>CCA411811962A4GALT,CYB5R3c.-49+27462A>G (n.-49+27462A>G)
c.617A>G (p.Asn206Ser)
gnomAD v4
22g.42693335T>GCA411811964A4GALT,CYB5R3c.-49+27462A>C (n.-49+27462A>C)
c.617A>C (p.Asn206Thr)
22g.42693336T>ACA411811966A4GALT,CYB5R3c.-49+27461A>T (n.-49+27461A>T)
c.616A>T (p.Asn206Tyr)
22g.42693336T>CCA411811968A4GALT,CYB5R3c.-49+27461A>G (n.-49+27461A>G)
c.616A>G (p.Asn206Asp)
22g.42693336T>GCA411811970A4GALT,CYB5R3c.-49+27461A>C (n.-49+27461A>C)
c.616A>C (p.Asn206His)
22g.42693337G>ACA515072395A4GALT,CYB5R3c.-49+27460C>T (n.-49+27460C>T)
c.615C>T (p.Thr205=)
22g.42693337G>CCA515072397A4GALT,CYB5R3c.-49+27460C>G (n.-49+27460C>G)
c.615C>G (p.Thr205=)
dbSNP
22g.42693337G=CA2406870246A4GALT,CYB5R3c.-49+27460C= (n.-49+27460C=)
c.615C= (p.Thr205=)
22g.42693337G>TCA515072394A4GALT,CYB5R3c.-49+27460C>A (n.-49+27460C>A)
c.615C>A (p.Thr205=)
22g.42693338G>ACA411811972A4GALT,CYB5R3c.-49+27459C>T (n.-49+27459C>T)
c.614C>T (p.Thr205Ile)
dbSNP
22g.42693338G>CCA411811975A4GALT,CYB5R3c.-49+27459C>G (n.-49+27459C>G)
c.614C>G (p.Thr205Ser)
22g.42693338G>TCA411811974A4GALT,CYB5R3c.-49+27459C>A (n.-49+27459C>A)
c.614C>A (p.Thr205Asn)
22g.42693339T>ACA411811981A4GALT,CYB5R3c.-49+27458A>T (n.-49+27458A>T)
c.613A>T (p.Thr205Ser)
22g.42693339T>CCA411811983A4GALT,CYB5R3c.-49+27458A>G (n.-49+27458A>G)
c.613A>G (p.Thr205Ala)
22g.42693339T>GCA411811985A4GALT,CYB5R3c.-49+27458A>C (n.-49+27458A>C)
c.613A>C (p.Thr205Pro)
22g.42693340C>ACA515072414A4GALT,CYB5R3c.-49+27457G>T (n.-49+27457G>T)
c.612G>T (p.Leu204=)
22g.42693340C>GCA515072408A4GALT,CYB5R3c.-49+27457G>C (n.-49+27457G>C)
c.612G>C (p.Leu204=)
gnomAD v4
22g.42693340C>TCA515072406A4GALT,CYB5R3c.-49+27457G>A (n.-49+27457G>A)
c.612G>A (p.Leu204=)
22g.42693341A=CA2406870247A4GALT,CYB5R3c.-49+27456T= (n.-49+27456T=)
c.611T= (p.Leu204=)
22g.42693341A>CCA324732289A4GALT,CYB5R3c.-49+27456T>G (n.-49+27456T>G)
c.611T>G (p.Leu204Arg)
dbSNP gnomAD v3 gnomAD v4
22g.42693341A>GCA411811988A4GALT,CYB5R3c.-49+27456T>C (n.-49+27456T>C)
c.611T>C (p.Leu204Pro)
22g.42693341A>TCA411811990A4GALT,CYB5R3c.-49+27456T>A (n.-49+27456T>A)
c.611T>A (p.Leu204Gln)
22g.42693342G>ACA515072419A4GALT,CYB5R3c.-49+27455C>T (n.-49+27455C>T)
c.610C>T (p.Leu204=)
dbSNP gnomAD v3 gnomAD v4
22g.42693342G>CCA411811993A4GALT,CYB5R3c.-49+27455C>G (n.-49+27455C>G)
c.610C>G (p.Leu204Val)
22g.42693342G=CA2406870248A4GALT,CYB5R3c.-49+27455C= (n.-49+27455C=)
c.610C= (p.Leu204=)
22g.42693342G>TCA411811994A4GALT,CYB5R3c.-49+27455C>A (n.-49+27455C>A)
c.610C>A (p.Leu204Met)
gnomAD v4
22g.42693343G>ACA515072422A4GALT,CYB5R3c.-49+27454C>T (n.-49+27454C>T)
c.609C>T (p.Asn203=)
gnomAD v4
22g.42693343G>CCA411811995A4GALT,CYB5R3c.-49+27454C>G (n.-49+27454C>G)
c.609C>G (p.Asn203Lys)
22g.42693343G>TCA411811996A4GALT,CYB5R3c.-49+27454C>A (n.-49+27454C>A)
c.609C>A (p.Asn203Lys)
22g.42693344T>ACA411811998A4GALT,CYB5R3c.-49+27453A>T (n.-49+27453A>T)
c.608A>T (p.Asn203Ile)
22g.42693344T>CCA411811999A4GALT,CYB5R3c.-49+27453A>G (n.-49+27453A>G)
c.608A>G (p.Asn203Ser)

Number of alleles fetched