Details for COL4A5:c.262C>T, p.Pro88Ser

CHROMOSOME X
GENOMIC COORDINATES
hg19hg38
107807142108563912
VARIANT EFFECT None
ANNOTATION FLAG None
GENE COL4A5
REFERENCE ALLELE C
ALTERNATE ALLELE T
TRANSCRIPT NM_033380.3
CDNA CHANGE c.262C>T
PROTEIN CHANGE p.Pro88Ser
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
7.679e-050.00.00.00.00094350.00.00.00022220.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedPossibly Damaging1.932651Polymorphism
DBSNP ID NA
1 combination linked to COL4A5:c.262C>T, p.Pro88Ser OLI1646
1 disease linked to COL4A5:c.262C>T, p.Pro88Ser Alport syndrome

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