Product Details

SNP ID

rs10776792

Assay Type

Functionally tested

NCBI dbSNP Submissions

71

Location

Chr.1:115033402 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCTGATGTCCATGCTTTTTGGCCTT[A/G]CATGTGGGCAAGCGATGTCTTTTTG

Phenotype

MIM: 188540

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

TSHB PubMed Links

Gene Details

Gene

TSHB

Gene Name

thyroid stimulating hormone beta

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000549.4	78	Missense Mutation	ACA,GCA	T14A	NP_000540.2
NM_001277991.1	78	Intron			NP_001264920.1
XM_011542065.2	78	Missense Mutation	ACA,GCA	T14A	XP_011540367.1

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