Details for LAMA3:c.1097G>A, p.Arg366His

CHROMOSOME 18
GENOMIC COORDINATES
hg19hg38
2147933923899375
VARIANT EFFECT missense
ANNOTATION FLAG automatically_attributed_and_verified
GENE LAMA3
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_000227.6
CDNA CHANGE c.1097G>A
PROTEIN CHANGE p.Arg366His
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
0.0010.00380.00.00.00.0

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
0.00020280.0027695.782e-050.00.00.03.517e-050.00.0

ESP
AAEA
0.0013620.0
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousBenign2.847702Polymorphism
DBSNP ID rs149809232
1 combination linked to LAMA3:c.1097G>A, p.Arg366His OLI576
1 disease linked to LAMA3:c.1097G>A, p.Arg366His Hypodontia

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