Details for HSPG2:c.10084C>T, p.Arg3362Cys

CHROMOSOME 1
GENOMIC COORDINATES
hg19hg38
2216538421838891
VARIANT EFFECT None
ANNOTATION FLAG None
GENE HSPG2
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_005529.7
CDNA CHANGE c.10084C>T
PROTEIN CHANGE p.Arg3362Cys
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
4.081e-050.00025928.761e-050.00.00.01.818e-050.00016740.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedDamaging3.787477Polymorphism
DBSNP ID NA
1 combination linked to HSPG2:c.10084C>T, p.Arg3362Cys OLI1679
1 disease linked to HSPG2:c.10084C>T, p.Arg3362Cys Non-Syndromic genetic keratoconus

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