Chr Mutation (hg38) CAid Gene Transcript Linkouts
22g.42693310_42693319delCA2577739307A4GALT,CYB5R3c.-49+27482_-49+27491del (n.-49+27482_-49+27491del)
c.637_646del (p.Arg213SerfsTer?)
22g.42693308A>CCA411811853A4GALT,CYB5R3c.-49+27489T>G (n.-49+27489T>G)
c.644T>G (p.Val215Gly)
22g.42693308A>GCA411811855A4GALT,CYB5R3c.-49+27489T>C (n.-49+27489T>C)
c.644T>C (p.Val215Ala)
22g.42693308A>TCA411811856A4GALT,CYB5R3c.-49+27489T>A (n.-49+27489T>A)
c.644T>A (p.Val215Asp)
22g.42693309C>ACA411811858A4GALT,CYB5R3c.-49+27488G>T (n.-49+27488G>T)
c.643G>T (p.Val215Phe)
22g.42693309C=CA2406870233A4GALT,CYB5R3c.-49+27488G= (n.-49+27488G=)
c.643G= (p.Val215=)
22g.42693309C>GCA10270250A4GALT,CYB5R3c.-49+27488G>C (n.-49+27488G>C)
c.643G>C (p.Val215Leu)
dbSNP ExAC gnomAD v2
22g.42693309C>TCA10270249A4GALT,CYB5R3c.-49+27488G>A (n.-49+27488G>A)
c.643G>A (p.Val215Ile)
dbSNP ExAC gnomAD v2 gnomAD v4
22g.42693310delCA2657079472A4GALT,CYB5R3c.-49+27487del (n.-49+27487del)
c.642del (p.Tyr214Ter)
gnomAD v4
22g.42693310G>ACA515072286A4GALT,CYB5R3c.-49+27487C>T (n.-49+27487C>T)
c.642C>T (p.Tyr214=)
dbSNP gnomAD v2 gnomAD v4
22g.42693310G>CCA411811861A4GALT,CYB5R3c.-49+27487C>G (n.-49+27487C>G)
c.642C>G (p.Tyr214Ter)
COSMIC
22g.42693310G=CA2406870234A4GALT,CYB5R3c.-49+27487C= (n.-49+27487C=)
c.642C= (p.Tyr214=)
22g.42693310G>TCA411811863A4GALT,CYB5R3c.-49+27487C>A (n.-49+27487C>A)
c.642C>A (p.Tyr214Ter)
gnomAD v4
22g.42693311T>ACA411811865A4GALT,CYB5R3c.-49+27486A>T (n.-49+27486A>T)
c.641A>T (p.Tyr214Phe)
22g.42693311T>CCA411811869A4GALT,CYB5R3c.-49+27486A>G (n.-49+27486A>G)
c.641A>G (p.Tyr214Cys)
dbSNP gnomAD v4
22g.42693311T>GCA411811866A4GALT,CYB5R3c.-49+27486A>C (n.-49+27486A>C)
c.641A>C (p.Tyr214Ser)
22g.42693311_42693312delCA2657079473A4GALT,CYB5R3c.-49+27485_-49+27486del (n.-49+27485_-49+27486del)
c.640_641del (p.Tyr214ArgfsTer?)
gnomAD v4
22g.42693312A=CA2406870235A4GALT,CYB5R3c.-49+27485T= (n.-49+27485T=)
c.640T= (p.Tyr214=)
22g.42693312A>CCA411811871A4GALT,CYB5R3c.-49+27485T>G (n.-49+27485T>G)
c.640T>G (p.Tyr214Asp)
22g.42693312A>GCA411811872A4GALT,CYB5R3c.-49+27485T>C (n.-49+27485T>C)
c.640T>C (p.Tyr214His)
22g.42693312A>TCA324732274A4GALT,CYB5R3c.-49+27485T>A (n.-49+27485T>A)
c.640T>A (p.Tyr214Asn)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
22g.42693312_42693322delinsAGCGGGACTGGCA2406870236A4GALT,CYB5R3c.-49+27475_-49+27485delinsCCAGTCCCGCT (n.-49+27475_-49+27485delinsCCAGTCCCGCT)
c.630_640delinsCCAGTCCCGCT (p.Thr210=)
22g.42693313G>ACA515072296A4GALT,CYB5R3c.-49+27484C>T (n.-49+27484C>T)
c.639C>T (p.Arg213=)
gnomAD v4
22g.42693313G>CCA515072297A4GALT,CYB5R3c.-49+27484C>G (n.-49+27484C>G)
c.639C>G (p.Arg213=)
22g.42693313G>TCA515072299A4GALT,CYB5R3c.-49+27484C>A (n.-49+27484C>A)
c.639C>A (p.Arg213=)
22g.42693314_42693321delCA2657079474A4GALT,CYB5R3c.-49+27477_-49+27484del (n.-49+27477_-49+27484del)
c.632_639del (p.Gln211LeufsTer?)
gnomAD v4
22g.42693314_42693323delCA639829272A4GALT,CYB5R3c.-49+27475_-49+27484del (n.-49+27475_-49+27484del)
c.630_639del (p.Gln211ThrfsTer?)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
22g.42693314C>ACA411811877A4GALT,CYB5R3c.-49+27483G>T (n.-49+27483G>T)
c.638G>T (p.Arg213Leu)
gnomAD v4
22g.42693314C=CA2406870237A4GALT,CYB5R3c.-49+27483G= (n.-49+27483G=)
c.638G= (p.Arg213=)
22g.42693314C>GCA411811879A4GALT,CYB5R3c.-49+27483G>C (n.-49+27483G>C)
c.638G>C (p.Arg213Pro)
22g.42693314C>TCA411811881A4GALT,CYB5R3c.-49+27483G>A (n.-49+27483G>A)
c.638G>A (p.Arg213His)
dbSNP gnomAD v4
22g.42693315G>ACA10270251A4GALT,CYB5R3c.-49+27482C>T (n.-49+27482C>T)
c.637C>T (p.Arg213Cys)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
22g.42693315G>CCA411811884A4GALT,CYB5R3c.-49+27482C>G (n.-49+27482C>G)
c.637C>G (p.Arg213Gly)
22g.42693315G=CA2406870238A4GALT,CYB5R3c.-49+27482C= (n.-49+27482C=)
c.637C= (p.Arg213=)
22g.42693315G>TCA411811887A4GALT,CYB5R3c.-49+27482C>A (n.-49+27482C>A)
c.637C>A (p.Arg213Ser)
22g.42693316G>ACA515072318A4GALT,CYB5R3c.-49+27481C>T (n.-49+27481C>T)
c.636C>T (p.Ser212=)
22g.42693316G>CCA515072317A4GALT,CYB5R3c.-49+27481C>G (n.-49+27481C>G)
c.636C>G (p.Ser212=)
22g.42693316G>TCA515072320A4GALT,CYB5R3c.-49+27481C>A (n.-49+27481C>A)
c.636C>A (p.Ser212=)
22g.42693317G>ACA411811891A4GALT,CYB5R3c.-49+27480C>T (n.-49+27480C>T)
c.635C>T (p.Ser212Phe)
COSMIC
22g.42693317G>CCA411811893A4GALT,CYB5R3c.-49+27480C>G (n.-49+27480C>G)
c.635C>G (p.Ser212Cys)
22g.42693317G>TCA411811889A4GALT,CYB5R3c.-49+27480C>A (n.-49+27480C>A)
c.635C>A (p.Ser212Tyr)
22g.42693318A>CCA411811894A4GALT,CYB5R3c.-49+27479T>G (n.-49+27479T>G)
c.634T>G (p.Ser212Ala)
22g.42693318A>GCA411811895A4GALT,CYB5R3c.-49+27479T>C (n.-49+27479T>C)
c.634T>C (p.Ser212Pro)
22g.42693318A>TCA411811897A4GALT,CYB5R3c.-49+27479T>A (n.-49+27479T>A)
c.634T>A (p.Ser212Thr)
22g.42693319C>ACA411811899A4GALT,CYB5R3c.-49+27478G>T (n.-49+27478G>T)
c.633G>T (p.Gln211His)
22g.42693319C>GCA411811900A4GALT,CYB5R3c.-49+27478G>C (n.-49+27478G>C)
c.633G>C (p.Gln211His)
22g.42693319C>TCA515072326A4GALT,CYB5R3c.-49+27478G>A (n.-49+27478G>A)
c.633G>A (p.Gln211=)
22g.42693320T>ACA411811902A4GALT,CYB5R3c.-49+27477A>T (n.-49+27477A>T)
c.632A>T (p.Gln211Leu)
22g.42693320T>CCA411811904A4GALT,CYB5R3c.-49+27477A>G (n.-49+27477A>G)
c.632A>G (p.Gln211Arg)
22g.42693320T>GCA411811906A4GALT,CYB5R3c.-49+27477A>C (n.-49+27477A>C)
c.632A>C (p.Gln211Pro)

Number of alleles fetched