Details for SRA1:c.59C>T, p.Pro20Leu

CHROMOSOME 5
GENOMIC COORDINATES
hg19hg38
139937015140557430
VARIANT EFFECT None
ANNOTATION FLAG None
GENE SRA1
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT NM_001035235.3
CDNA CHANGE c.59C>T
PROTEIN CHANGE p.Pro20Leu
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
9.655e-050.03.735e-050.00.00015820.00.00014990.00021117.631e-05

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousDamaging4.972382Disease causing
DBSNP ID NA
1 combination linked to SRA1:c.59C>T, p.Pro20Leu OLI1568
1 disease linked to SRA1:c.59C>T, p.Pro20Leu Syndrome with 46,XY disorder of sex development

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