Details for TSC1:

CHROMOSOME 9
GENOMIC COORDINATES
hg19hg38
135786863132911476
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
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
5.57e-050.00043065.782e-050.00029770.00.08.802e-060.0001630.0

ESP
AAEA
0.00068090.0
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousBenign3.396451Polymorphism
DBSNP ID NA
1 combination linked to TSC1: OLI485
1 disease linked to TSC1: Rare pervasive developmental disorder

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