Details for HOXA11:c.304G>A, p.Val102Met

CHROMOSOME 7
GENOMIC COORDINATES
hg19hg38
2722446027184841
VARIANT EFFECT missense
ANNOTATION FLAG manually_attributed
GENE HOXA11
REFERENCE ALLELE C
ALTERNATE ALLELE T
TRANSCRIPT NM_005523.5
CDNA CHANGE c.304G>A
PROTEIN CHANGE p.Val102Met
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
8.05e-060.00.00.00.00.00.00.06.545e-05

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedBenign2.820022Disease causing
DBSNP ID rs780070206
1 combination linked to HOXA11:c.304G>A, p.Val102Met OLI797
1 disease linked to HOXA11:c.304G>A, p.Val102Met Arthrogryposis syndrome

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