Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.73322525C>ACA393084787HCN4c.3568G>T (p.Ala1190Ser)
c.2350G>T (p.Ala784Ser)
gnomAD v4
15g.73322525C=CA2187186155HCN4c.3568G= (p.Ala1190=)
c.2350G= (p.Ala784=)
15g.73322525C>GCA393084790HCN4c.3568G>C (p.Ala1190Pro)
c.2350G>C (p.Ala784Pro)
15g.73322525C>TCA16614725HCN4c.3568G>A (p.Ala1190Thr)
c.2350G>A (p.Ala784Thr)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73322526C>ACA491477844HCN4c.3567G>T (p.Gly1189=)
c.2349G>T (p.Gly783=)
gnomAD v4
15g.73322526C=CA2187186158HCN4c.3567G= (p.Gly1189=)
c.2349G= (p.Gly783=)
15g.73322526C>GCA491477845HCN4c.3567G>C (p.Gly1189=)
c.2349G>C (p.Gly783=)
gnomAD v4
15g.73322526C>TCA7648804HCN4c.3567G>A (p.Gly1189=)
c.2349G>A (p.Gly783=)
dbSNP ExAC gnomAD v2 gnomAD v4
15g.73322527C>ACA393084794HCN4c.3566G>T (p.Gly1189Val)
c.2348G>T (p.Gly783Val)
gnomAD v4
15g.73322527C=CA2187186161HCN4c.3566G= (p.Gly1189=)
c.2348G= (p.Gly783=)
15g.73322527C>GCA393084797HCN4c.3566G>C (p.Gly1189Ala)
c.2348G>C (p.Gly783Ala)
15g.73322527C>TCA393084800HCN4c.3566G>A (p.Gly1189Glu)
c.2348G>A (p.Gly783Glu)
dbSNP gnomAD v2
15g.73322528C>ACA393084804HCN4c.3565G>T (p.Gly1189Trp)
c.2347G>T (p.Gly783Trp)
dbSNP gnomAD v2 gnomAD v4
15g.73322528C=CA2187186164HCN4c.3565G= (p.Gly1189=)
c.2347G= (p.Gly783=)
15g.73322528C>GCA393084806HCN4c.3565G>C (p.Gly1189Arg)
c.2347G>C (p.Gly783Arg)
15g.73322528C>TCA393084810HCN4c.3565G>A (p.Gly1189Arg)
c.2347G>A (p.Gly783Arg)
15g.73322529A>CCA491477851HCN4c.3564T>G (p.Pro1188=)
c.2346T>G (p.Pro782=)
15g.73322529A>GCA491477849HCN4c.3564T>C (p.Pro1188=)
c.2346T>C (p.Pro782=)
15g.73322529A>TCA491477850HCN4c.3564T>A (p.Pro1188=)
c.2346T>A (p.Pro782=)
15g.73322530G>ACA393084813HCN4c.3563C>T (p.Pro1188Leu)
c.2345C>T (p.Pro782Leu)
COSMIC
15g.73322530G>CCA393084815HCN4c.3563C>G (p.Pro1188Arg)
c.2345C>G (p.Pro782Arg)
gnomAD v4
15g.73322530G>TCA393084816HCN4c.3563C>A (p.Pro1188His)
c.2345C>A (p.Pro782His)
15g.73322531G>ACA393084819HCN4c.3562C>T (p.Pro1188Ser)
c.2344C>T (p.Pro782Ser)
15g.73322531G>CCA393084821HCN4c.3562C>G (p.Pro1188Ala)
c.2344C>G (p.Pro782Ala)
15g.73322531G>TCA393084824HCN4c.3562C>A (p.Pro1188Thr)
c.2344C>A (p.Pro782Thr)
gnomAD v4
15g.73322532T>ACA393084828HCN4c.3561A>T (p.Glu1187Asp)
c.2343A>T (p.Glu781Asp)
15g.73322532T>CCA491477855HCN4c.3561A>G (p.Glu1187=)
c.2343A>G (p.Glu781=)
dbSNP gnomAD v3 gnomAD v4
15g.73322532T>GCA393084825HCN4c.3561A>C (p.Glu1187Asp)
c.2343A>C (p.Glu781Asp)
15g.73322532T=CA2187186167HCN4c.3561A= (p.Glu1187=)
c.2343A= (p.Glu781=)
15g.73322533T>ACA393084831HCN4c.3560A>T (p.Glu1187Val)
c.2342A>T (p.Glu781Val)
15g.73322533T>CCA393084834HCN4c.3560A>G (p.Glu1187Gly)
c.2342A>G (p.Glu781Gly)
15g.73322533T>GCA393084835HCN4c.3560A>C (p.Glu1187Ala)
c.2342A>C (p.Glu781Ala)
15g.73322534C>ACA393084839HCN4c.3559G>T (p.Glu1187Ter)
c.2341G>T (p.Glu781Ter)
15g.73322534C>GCA393084842HCN4c.3559G>C (p.Glu1187Gln)
c.2341G>C (p.Glu781Gln)
15g.73322534C>TCA393084844HCN4c.3559G>A (p.Glu1187Lys)
c.2341G>A (p.Glu781Lys)
15g.73322535C>ACA393084849HCN4c.3558G>T (p.Arg1186Ser)
c.2340G>T (p.Arg780Ser)
15g.73322535C>GCA393084850HCN4c.3558G>C (p.Arg1186Ser)
c.2340G>C (p.Arg780Ser)
15g.73322535C>TCA491477858HCN4c.3558G>A (p.Arg1186=)
c.2340G>A (p.Arg780=)
ClinVar gnomAD v4
15g.73322536C>ACA393084851HCN4c.3557G>T (p.Arg1186Met)
c.2339G>T (p.Arg780Met)
15g.73322536C=CA2187186169HCN4c.3557G= (p.Arg1186=)
c.2339G= (p.Arg780=)
15g.73322536C>GCA393084853HCN4c.3557G>C (p.Arg1186Thr)
c.2339G>C (p.Arg780Thr)
15g.73322536C>TCA393084855HCN4c.3557G>A (p.Arg1186Lys)
c.2339G>A (p.Arg780Lys)
dbSNP gnomAD v2 gnomAD v4
15g.73322537T>ACA393084858HCN4c.3556A>T (p.Arg1186Trp)
c.2338A>T (p.Arg780Trp)
15g.73322537T>CCA393084859HCN4c.3556A>G (p.Arg1186Gly)
c.2338A>G (p.Arg780Gly)
15g.73322537T>GCA491477862HCN4c.3556A>C (p.Arg1186=)
c.2338A>C (p.Arg780=)
15g.73322538C>ACA393084867HCN4c.3555G>T (p.Gln1185His)
c.2337G>T (p.Gln779His)
gnomAD v4
15g.73322538C>GCA393084864HCN4c.3555G>C (p.Gln1185His)
c.2337G>C (p.Gln779His)
15g.73322538C>TCA491477863HCN4c.3555G>A (p.Gln1185=)
c.2337G>A (p.Gln779=)
ClinVar gnomAD v4
15g.73322539T>ACA393084870HCN4c.3554A>T (p.Gln1185Leu)
c.2336A>T (p.Gln779Leu)
dbSNP
15g.73322539T>CCA393084871HCN4c.3554A>G (p.Gln1185Arg)
c.2336A>G (p.Gln779Arg)

Number of alleles fetched