Chr Mutation (hg38) CAid Gene Transcript Linkouts
22g.27750934A>CCA411032756MN1n.469T>G
c.3944T>G (p.Phe1315Cys)
c.297T>G
n.300T>G
22g.27750934A>GCA411032758MN1n.469T>C
c.3944T>C (p.Phe1315Ser)
c.297T>C
n.300T>C
22g.27750934A>TCA411032760MN1n.469T>A
c.3944T>A (p.Phe1315Tyr)
c.297T>A
n.300T>A
22g.27750934_27750935insGCCTCA2655934854MN1n.468_469insAGGC
c.3943_3944insAGGC (p.Phe1315Ter)
c.296_297insAGGC
n.299_300insAGGC
 gnomAD v4
22g.27750935A>CCA411032762MN1n.468T>G
c.3943T>G (p.Phe1315Val)
c.296T>G
n.299T>G
22g.27750935A>GCA411032764MN1n.468T>C
c.3943T>C (p.Phe1315Leu)
c.296T>C
n.299T>C
22g.27750935A>TCA411032766MN1n.468T>A
c.3943T>A (p.Phe1315Ile)
c.296T>A
n.299T>A
22g.27750936T>ACA513939233MN1n.467A>T
c.3942A>T (p.Thr1314=)
c.295A>T
n.298A>T
22g.27750936T>CCA513939234MN1n.467A>G
c.3942A>G (p.Thr1314=)
c.295A>G
n.298A>G
 gnomAD v4
22g.27750936T>GCA513939235MN1n.467A>C
c.3942A>C (p.Thr1314=)
c.295A>C
n.298A>C
22g.27750937G>ACA411032769MN1n.466C>T
c.3941C>T (p.Thr1314Ile)
c.294C>T
n.297C>T
 COSMIC
22g.27750937G>CCA411032771MN1n.466C>G
c.3941C>G (p.Thr1314Arg)
c.294C>G
n.297C>G
22g.27750937G=CA2399818101MN1n.466C=
c.3941C= (p.Thr1314=)
c.294C=
n.297C=
22g.27750937G>TCA411032772MN1n.466C>A
c.3941C>A (p.Thr1314Lys)
c.294C>A
n.297C>A
 dbSNP gnomAD v2 gnomAD v4
22g.27750938T>ACA411032775MN1n.465A>T
c.3940A>T (p.Thr1314Ser)
c.293A>T
n.296A>T
22g.27750938T>CCA10165932MN1n.465A>G
c.3940A>G (p.Thr1314Ala)
c.293A>G
n.296A>G
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
22g.27750938T>GCA411032778MN1n.465A>C
c.3940A>C (p.Thr1314Pro)
c.293A>C
n.296A>C
22g.27750938T=CA2399818102MN1n.465A=
c.3940A= (p.Thr1314=)
c.293A=
n.296A=
22g.27750939C>ACA513939236MN1n.464G>T
c.3939G>T (p.Gly1313=)
c.292G>T
n.295G>T
 gnomAD v4
22g.27750939C>GCA513939237MN1n.464G>C
c.3939G>C (p.Gly1313=)
c.292G>C
n.295G>C
22g.27750939C>TCA513939238MN1n.464G>A
c.3939G>A (p.Gly1313=)
c.292G>A
n.295G>A
22g.27750940C>ACA411032783MN1n.463G>T
c.3938G>T (p.Gly1313Val)
c.291G>T
n.294G>T
 gnomAD v4
22g.27750940C>GCA411032781MN1n.463G>C
c.3938G>C (p.Gly1313Ala)
c.291G>C
n.294G>C
22g.27750940C>TCA411032779MN1n.463G>A
c.3938G>A (p.Gly1313Glu)
c.291G>A
n.294G>A
22g.27750941C>ACA411032785MN1n.462G>T
c.3937G>T (p.Gly1313Trp)
c.290G>T
n.293G>T
 gnomAD v4
22g.27750941C=CA2399818103MN1n.462G=
c.3937G= (p.Gly1313=)
c.290G=
n.293G=
22g.27750941C>GCA411032786MN1n.462G>C
c.3937G>C (p.Gly1313Arg)
c.290G>C
n.293G>C
22g.27750941C>TCA411032788MN1n.462G>A
c.3937G>A (p.Gly1313Arg)
c.290G>A
n.293G>A
 dbSNP
22g.27750942A>CCA411032791MN1n.461T>G
c.3936T>G (p.Phe1312Leu)
c.289T>G
n.292T>G
22g.27750942A>GCA513939239MN1n.461T>C
c.3936T>C (p.Phe1312=)
c.289T>C
n.292T>C
22g.27750942A>TCA411032792MN1n.461T>A
c.3936T>A (p.Phe1312Leu)
c.289T>A
n.292T>A
22g.27750943A>CCA411032795MN1n.460T>G
c.3935T>G (p.Phe1312Cys)
c.288T>G
n.291T>G
22g.27750943A>GCA411032797MN1n.460T>C
c.3935T>C (p.Phe1312Ser)
c.288T>C
n.291T>C
22g.27750943A>TCA411032799MN1n.460T>A
c.3935T>A (p.Phe1312Tyr)
c.288T>A
n.291T>A
22g.27750944A=CA2399818104MN1n.459T=
c.3934T= (p.Phe1312=)
c.287T=
n.290T=
22g.27750944A>CCA411032801MN1n.459T>G
c.3934T>G (p.Phe1312Val)
c.287T>G
n.290T>G
22g.27750944A>GCA411032802MN1n.459T>C
c.3934T>C (p.Phe1312Leu)
c.287T>C
n.290T>C
 dbSNP gnomAD v3 gnomAD v4
22g.27750944A>TCA411032803MN1n.459T>A
c.3934T>A (p.Phe1312Ile)
c.287T>A
n.290T>A
22g.27750945T>ACA411032805MN1n.458A>T
c.3933A>T (p.Arg1311Ser)
c.286A>T
n.289A>T
22g.27750945T>CCA513939240MN1n.458A>G
c.3933A>G (p.Arg1311=)
c.286A>G
n.289A>G
22g.27750945T>GCA411032807MN1n.458A>C
c.3933A>C (p.Arg1311Ser)
c.286A>C
n.289A>C
22g.27750946C>ACA411032809MN1n.457G>T
c.3932G>T (p.Arg1311Ile)
c.285G>T
n.288G>T
 gnomAD v4
22g.27750946C=CA2399818105MN1n.457G=
c.3932G= (p.Arg1311=)
c.285G=
n.288G=
22g.27750946C>GCA411032811MN1n.457G>C
c.3932G>C (p.Arg1311Thr)
c.285G>C
n.288G>C
22g.27750946C>TCA322870756MN1n.457G>A
c.3932G>A (p.Arg1311Lys)
c.285G>A
n.288G>A
 dbSNP
22g.27750947T>ACA411032814MN1n.456A>T
c.3931A>T (p.Arg1311Ter)
c.284A>T
n.287A>T
22g.27750947T>CCA411032816MN1n.456A>G
c.3931A>G (p.Arg1311Gly)
c.284A>G
n.287A>G
22g.27750947T>GCA513939241MN1n.456A>C
c.3931A>C (p.Arg1311=)
c.284A>C
n.287A>C
22g.27750948G>ACA10165933MN1n.455C>T
c.3930C>T (p.Asn1310=)
c.283C>T
n.286C>T
 dbSNP ExAC gnomAD v2 gnomAD v4
22g.27750948G>CCA411032822MN1n.455C>G
c.3930C>G (p.Asn1310Lys)
c.283C>G
n.286C>G

Number of alleles fetched