Details for ERBB4:c.1879G>A, p.Gly627Ser

CHROMOSOME 2
GENOMIC COORDINATES
hg19hg38
212522546211657821
VARIANT EFFECT None
ANNOTATION FLAG None
GENE ERBB4
REFERENCE ALLELE C
ALTERNATE ALLELE T
TRANSCRIPT NM_005235.3
CDNA CHANGE c.1879G>A
PROTEIN CHANGE p.Gly627Ser
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
7.953e-060.00.00.00.00.01.758e-050.00.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedPossibly Damaging3.414225Polymorphism
DBSNP ID NA
1 combination linked to ERBB4:c.1879G>A, p.Gly627Ser OLI1639
1 disease linked to ERBB4:c.1879G>A, p.Gly627Ser Amyotrophic lateral sclerosis

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