Details for VLDLR:c.1313G>A, p.Gly438Asp

CHROMOSOME 9
GENOMIC COORDINATES
hg19hg38
26455742645574
VARIANT EFFECT None
ANNOTATION FLAG None
GENE VLDLR
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_003383
CDNA CHANGE c.1313G>A
PROTEIN CHANGE p.Gly438Asp
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
0.00120.00.00860.00.00.0

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
0.0004220.00.0030350.00.00.00.00.00016320.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging4.675237Disease causing
DBSNP ID NA
1 combination linked to VLDLR:c.1313G>A, p.Gly438Asp OLI1466
1 disease linked to VLDLR:c.1313G>A, p.Gly438Asp Rare pervasive developmental disorder

Found any issues with the data on this page? Report this entry.