Details for TSC2:

CHROMOSOME 16
GENOMIC COORDINATES
hg19hg38
21144262064425
VARIANT EFFECT missense
ANNOTATION FLAG manually_attributed
GENE TSC2
REFERENCE ALLELE A
ALTERNATE ALLELE C
TRANSCRIPT N.A.
CDNA CHANGE None
PROTEIN CHANGE None
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousPossibly Damaging4.093484Polymorphism
DBSNP ID NA
1 combination linked to TSC2: OLI496
1 disease linked to TSC2: Rare pervasive developmental disorder

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