Details for PRMT7:c.1097G>A, p.Cys366Tyr

CHROMOSOME 16
GENOMIC COORDINATES
hg19hg38
6838008968346186
VARIANT EFFECT None
ANNOTATION FLAG None
GENE PRMT7
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT N.A.
CDNA CHANGE c.1097G>A
PROTEIN CHANGE p.Cys366Tyr
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging4.02411Disease causing
DBSNP ID NA
1 combination linked to PRMT7:c.1097G>A, p.Cys366Tyr OLI1028
1 disease linked to PRMT7:c.1097G>A, p.Cys366Tyr Short stature-brachydactyly-obesity-global developmental delay syndrome

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