Details for TSC1:

CHROMOSOME 9
GENOMIC COORDINATES
hg19hg38
135786013132910626
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
0.00020.00.00.0010.00.0

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
0.00034650.00030790.00011560.00.00016329.267e-050.0006080.00016339.799e-05

ESP
AAEA
0.00045390.0006977
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedBenign2.177666Polymorphism
DBSNP ID NA
1 combination linked to TSC1: OLI478
1 disease linked to TSC1: Rare pervasive developmental disorder

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