Details for FAM83H:c.1498C>G, p.Leu500Val

CHROMOSOME 8
GENOMIC COORDINATES
hg19hg38
144810133143727963
VARIANT EFFECT None
ANNOTATION FLAG None
GENE FAM83H
REFERENCE ALLELE G
ALTERNATE ALLELE C
TRANSCRIPT NM_198488.5
CDNA CHANGE c.1498C>G
PROTEIN CHANGE p.Leu500Val
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousPossibly Damaging2.269259Polymorphism
DBSNP ID NA
1 combination linked to FAM83H:c.1498C>G, p.Leu500Val OLI1736
1 disease linked to FAM83H:c.1498C>G, p.Leu500Val Amelogenesis imperfecta

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