Details for TSHR:c.611C>T, p.Ala204Val

CHROMOSOME 14
GENOMIC COORDINATES
hg19hg38
8156304881096704
VARIANT EFFECT None
ANNOTATION FLAG None
GENE TSHR
REFERENCE ALLELE C
ALTERNATE ALLELE T
TRANSCRIPT N.A.
CDNA CHANGE c.611C>T
PROTEIN CHANGE p.Ala204Val
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
1.992e-050.00.00.00.00027190.00.00.00.0

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
DeleteriousPossibly Damaging3.620092Disease causing
DBSNP ID NA
1 combination linked to TSHR:c.611C>T, p.Ala204Val OLI1494
1 disease linked to TSHR:c.611C>T, p.Ala204Val Congenital hypothyroidism

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