Details for ARHGEF10:c.700C>A, p.Pro234Thr

CHROMOSOME 8
GENOMIC COORDINATES
hg19hg38
18173621869196
VARIANT EFFECT missense
ANNOTATION FLAG automatically_attributed_and_verified
GENE ARHGEF10
REFERENCE ALLELE C
ALTERNATE ALLELE A
TRANSCRIPT NM_001308153.2
CDNA CHANGE c.700C>A
PROTEIN CHANGE p.Pro234Thr
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
3.976e-060.00.00.00.00.08.791e-060.00.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousPossibly Damaging2.735101Polymorphism
DBSNP ID rs545402502
1 combination linked to ARHGEF10:c.700C>A, p.Pro234Thr OLI331
1 disease linked to ARHGEF10:c.700C>A, p.Pro234Thr Amyotrophic lateral sclerosis

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