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Details for TSHR:p.Ser562Gly

CHROMOSOME

14

GENOMIC COORDINATES

hg19	hg38
81610086	81143742

VARIANT EFFECT

missense

ANNOTATION FLAG

automatically_attributed

GENE

REFERENCE ALLELE

A

ALTERNATE ALLELE

G

TRANSCRIPT

N.A.

CDNA CHANGE

None

PROTEIN CHANGE

p.Ser562Gly

ALLELE FREQUENCY

1KGP
Global	AFR	AMR	EAS	EUR	SAS
None	None	None	None	None	None

Gnomad
Global	AFR	AMR	ASJ	EAS	FIN	NFE	OTH	SAS
None	None	None	None	None	None	None	None	None

ESP
AA	EA
None	None

PREDICTORS

sift	pp2 hvar	cadd	mutationtaster
Deleterious	Damaging	3.78388	Disease causing

DBSNP ID

1 combination linked to TSHR:p.Ser562Gly

1 disease linked to TSHR:p.Ser562Gly

Congenital hypothyroidism

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