Details for LOXL2:c.1642C>A, p.Pro548Thr

CHROMOSOME 8
GENOMIC COORDINATES
hg19hg38
2316741923309906
VARIANT EFFECT None
ANNOTATION FLAG None
GENE LOXL2
REFERENCE ALLELE G
ALTERNATE ALLELE T
TRANSCRIPT NM_002318.3
CDNA CHANGE c.1642C>A
PROTEIN CHANGE p.Pro548Thr
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging3.346567Disease causing
DBSNP ID NA
1 combination linked to LOXL2:c.1642C>A, p.Pro548Thr OLI1674
1 disease linked to LOXL2:c.1642C>A, p.Pro548Thr Non-Syndromic genetic keratoconus

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