Details for HSPG2:c.2023C>T, p.Arg675Trp

CHROMOSOME 1
GENOMIC COORDINATES
hg19hg38
2220702821880535
VARIANT EFFECT None
ANNOTATION FLAG None
GENE HSPG2
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_005529.7
CDNA CHANGE c.2023C>T
PROTEIN CHANGE p.Arg675Trp
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
8.852e-050.000252.905e-050.00.00021880.00.00010690.00016460.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousPossibly Damaging4.020179Polymorphism
DBSNP ID NA
1 combination linked to HSPG2:c.2023C>T, p.Arg675Trp OLI1676
1 disease linked to HSPG2:c.2023C>T, p.Arg675Trp Syndromic genetic keratoconus

Found any issues with the data on this page? Report this entry.