Details for SEMA3A:c.869G>A, p.Arg290His

CHROMOSOME 7
GENOMIC COORDINATES
hg19hg38
8364055584011239
VARIANT EFFECT missense
ANNOTATION FLAG automatically_attributed
GENE SEMA3A
REFERENCE ALLELE C
ALTERNATE ALLELE T
TRANSCRIPT NM_006080.2
CDNA CHANGE c.869G>A
PROTEIN CHANGE p.Arg290His
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
2.389e-050.00018460.09.927e-050.00.01.762e-050.00.0

ESP
AAEA
0.0002270.0001163
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging4.236329Disease causing
DBSNP ID rs140824469
1 combination linked to SEMA3A:c.869G>A, p.Arg290His OLI881
1 disease linked to SEMA3A:c.869G>A, p.Arg290His Kallmann syndrome

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