Details for SRA1:c.218C>T, p.Pro73Leu

CHROMOSOME 5
GENOMIC COORDINATES
hg19hg38
139931703140552118
VARIANT EFFECT None
ANNOTATION FLAG None
GENE SRA1
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_001035235
CDNA CHANGE c.218C>T
PROTEIN CHANGE p.Pro73Leu
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedBenign1.999472Polymorphism
DBSNP ID NA
1 combination linked to SRA1:c.218C>T, p.Pro73Leu OLI1566
1 disease linked to SRA1:c.218C>T, p.Pro73Leu Syndrome with 46,XY disorder of sex development

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