Details for HMCN1:c.109G>A,

CHROMOSOME 1
GENOMIC COORDINATES
hg19hg38
185704020185734888
VARIANT EFFECT None
ANNOTATION FLAG None
GENE HMCN1
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_031935.3
CDNA CHANGE c.109G>A
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
0.00013520.02.891e-050.00.09.239e-050.00026370.00016290.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedBenign3.120711Polymorphism
DBSNP ID NA
1 combination linked to HMCN1:c.109G>A, OLI1333
1 disease linked to HMCN1:c.109G>A, Primary immunodeficiency

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