Details for LAMA3:c.2798G>T, p.Gly933Val

CHROMOSOME 18
GENOMIC COORDINATES
hg19hg38
2149480523914841
VARIANT EFFECT missense
ANNOTATION FLAG automatically_attributed_and_verified
GENE LAMA3
REFERENCE ALLELE G
ALTERNATE ALLELE T
TRANSCRIPT NM_000227.6
CDNA CHANGE c.2798G>T
PROTEIN CHANGE p.Gly933Val
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging4.186988Disease causing
DBSNP ID rs1434986565
1 combination linked to LAMA3:c.2798G>T, p.Gly933Val OLI577
1 disease linked to LAMA3:c.2798G>T, p.Gly933Val Hypodontia

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