Details for TSC1:

CHROMOSOME 9
GENOMIC COORDINATES
hg19hg38
135779052132903665
VARIANT EFFECT missense
ANNOTATION FLAG manually_attributed
GENE TSC1
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT N.A.
CDNA CHANGE None
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
0.00140.00.00140.00.0060.0

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
0.003640.00098440.0012140.00.00.013770.0047430.0032670.0

ESP
AAEA
0.00090790.003605
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousPossibly Damaging3.959204Polymorphism
DBSNP ID NA
1 combination linked to TSC1: OLI488
1 disease linked to TSC1: Rare pervasive developmental disorder

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