Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.212858813A=CA1143538525FLVCR1c.361A= (p.Asn121=)
n.535A=
1g.212858813A>CCA344795880FLVCR1c.361A>C (p.Asn121His)
n.535A>C
1g.212858813A>GCA115240FLVCR1c.361A>G (p.Asn121Asp)
n.535A>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.212858813A>TCA344795881FLVCR1c.361A>T (p.Asn121Tyr)
n.535A>T
1g.212858814A=CA2485633255FLVCR1c.362A= (p.Asn121=)
n.536A=
1g.212858814A>CCA344795882FLVCR1c.362A>C (p.Asn121Thr)
n.536A>C
gnomAD v4
1g.212858814A>GCA36897026FLVCR1c.362A>G (p.Asn121Ser)
n.536A>G
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.212858814A>TCA344795883FLVCR1c.362A>T (p.Asn121Ile)
n.536A>T
gnomAD v4
1g.212858815C>ACA344795884FLVCR1c.363C>A (p.Asn121Lys)
n.537C>A
1g.212858815C>GCA344795885FLVCR1c.363C>G (p.Asn121Lys)
n.537C>G
1g.212858815C>TCA423422808FLVCR1c.363C>T (p.Asn121=)
n.537C>T
gnomAD v4
1g.212858816G>ACA344795886FLVCR1c.364G>A (p.Ala122Thr)
n.538G>A
ClinVar dbSNP gnomAD v4
1g.212858816G>CCA344795887FLVCR1c.364G>C (p.Ala122Pro)
n.538G>C
1g.212858816G=CA2485633256FLVCR1c.364G= (p.Ala122=)
n.538G=
1g.212858816G>TCA344795888FLVCR1c.364G>T (p.Ala122Ser)
n.538G>T
1g.212858817C>ACA344795889FLVCR1c.365C>A (p.Ala122Asp)
n.539C>A
1g.212858817C=CA2485633257FLVCR1c.365C= (p.Ala122=)
n.539C=
1g.212858817C>GCA344795891FLVCR1c.365C>G (p.Ala122Gly)
n.539C>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.212858817C>TCA344795890FLVCR1c.365C>T (p.Ala122Val)
n.539C>T
dbSNP
1g.212858818C>ACA423422809FLVCR1c.366C>A (p.Ala122=)
n.540C>A
1g.212858818C=CA1144019717FLVCR1c.366C= (p.Ala122=)
n.540C=
1g.212858818C>GCA36897031FLVCR1c.366C>G (p.Ala122=)
n.540C>G
dbSNP gnomAD v4
1g.212858818C>TCA1385885FLVCR1c.366C>T (p.Ala122=)
n.540C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
1g.212858819T>ACA344795893FLVCR1c.367T>A (p.Phe123Ile)
n.541T>A
1g.212858819T>CCA344795892FLVCR1c.367T>C (p.Phe123Leu)
n.541T>C
1g.212858819T>GCA344795894FLVCR1c.367T>G (p.Phe123Val)
n.541T>G
1g.212858820T>ACA344795895FLVCR1c.368T>A (p.Phe123Tyr)
n.542T>A
1g.212858820T>CCA344795896FLVCR1c.368T>C (p.Phe123Ser)
n.542T>C
1g.212858820T>GCA344795897FLVCR1c.368T>G (p.Phe123Cys)
n.542T>G
dbSNP gnomAD v4
1g.212858820T=CA2485633258FLVCR1c.368T= (p.Phe123=)
n.542T=
1g.212858821T>ACA344795898FLVCR1c.369T>A (p.Phe123Leu)
n.543T>A
ClinVar dbSNP gnomAD v4
1g.212858821T>CCA423422810FLVCR1c.369T>C (p.Phe123=)
n.543T>C
1g.212858821T>GCA344795899FLVCR1c.369T>G (p.Phe123Leu)
n.543T>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.212858821T=CA2485633259FLVCR1c.369T= (p.Phe123=)
n.543T=
1g.212858822C>ACA344795900FLVCR1c.370C>A (p.Gln124Lys)
n.544C>A
1g.212858822C>GCA344795901FLVCR1c.370C>G (p.Gln124Glu)
n.544C>G
gnomAD v4
1g.212858822C>TCA344795902FLVCR1c.370C>T (p.Gln124Ter)
n.544C>T
1g.212858823A=CA2485633260FLVCR1c.371A= (p.Gln124=)
n.545A=
1g.212858823A>CCA344795903FLVCR1c.371A>C (p.Gln124Pro)
n.545A>C
1g.212858823A>GCA344795904FLVCR1c.371A>G (p.Gln124Arg)
n.545A>G
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.212858823A>TCA344795905FLVCR1c.371A>T (p.Gln124Leu)
n.545A>T
dbSNP
1g.212858824G>ACA423422811FLVCR1c.372G>A (p.Gln124=)
n.546G>A
ClinVar dbSNP COSMIC
1g.212858824G>CCA344795907FLVCR1c.372G>C (p.Gln124His)
n.546G>C
1g.212858824G=CA2485633261FLVCR1c.372G= (p.Gln124=)
n.546G=
1g.212858824G>TCA344795906FLVCR1c.372G>T (p.Gln124His)
n.546G>T
1g.212858825_212858827delCA2650435905FLVCR1c.373_375del (p.Trp125del)
n.547_549del
gnomAD v4
1g.212858825T>ACA344795908FLVCR1c.373T>A (p.Trp125Arg)
n.547T>A
dbSNP gnomAD v2 gnomAD v4
1g.212858825T>CCA344795909FLVCR1c.373T>C (p.Trp125Arg)
n.547T>C
1g.212858825T>GCA344795910FLVCR1c.373T>G (p.Trp125Gly)
n.547T>G
1g.212858825T=CA2485633262FLVCR1c.373T= (p.Trp125=)
n.547T=

Number of alleles fetched