Details for ALDH1L1:c.2266C>G, p.His756Asp

CHROMOSOME 3
GENOMIC COORDINATES
hg19hg38
125828898126110055
VARIANT EFFECT missense
ANNOTATION FLAG automatically_attributed_and_verified
GENE ALDH1L1
REFERENCE ALLELE G
ALTERNATE ALLELE C
TRANSCRIPT NM_001270364.2
CDNA CHANGE c.2266C>G
PROTEIN CHANGE p.His756Asp
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
3.977e-050.00.00.00.00.08.791e-050.00.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging3.290786Disease causing
DBSNP ID rs775766256
1 combination linked to ALDH1L1:c.2266C>G, p.His756Asp OLI703
1 disease linked to ALDH1L1:c.2266C>G, p.His756Asp Isolated anencephaly

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