Details for HMCN1:c.4586A>G,

CHROMOSOME 1
GENOMIC COORDINATES
hg19hg38
185976370186007238
VARIANT EFFECT None
ANNOTATION FLAG None
GENE HMCN1
REFERENCE ALLELE A
ALTERNATE ALLELE G
TRANSCRIPT NM_031935.3
CDNA CHANGE c.4586A>G
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
0.00140.00.00290.00.0050.0

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
0.0058960.00092310.0020550.0024840.00.011320.0088590.0062110.002646

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedDamaging2.968984Polymorphism
DBSNP ID NA
1 combination linked to HMCN1:c.4586A>G, OLI1333
1 disease linked to HMCN1:c.4586A>G, Primary immunodeficiency

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