Details for TSC2:

CHROMOSOME 16
GENOMIC COORDINATES
hg19hg38
21129892062988
VARIANT EFFECT missense
ANNOTATION FLAG manually_attributed
GENE TSC2
REFERENCE ALLELE G
ALTERNATE ALLELE A
TRANSCRIPT N.A.
CDNA CHANGE None
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
0.0012450.00022930.00024250.013148.848e-050.00.00073260.0061228.777e-05

ESP
AAEA
0.00025730.001084
PREDICTORS
siftpp2 hvarcaddmutationtaster
ToleratedPossibly Damaging3.04488Polymorphism
DBSNP ID NA
1 combination linked to TSC2: OLI484
1 disease linked to TSC2: Rare pervasive developmental disorder

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