Product Details

SNP ID

rs1127958

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:150801721 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCAGCAGCCGGCTGCTGGTGGCCTC[A/G]TGGGTGAGTGTGACGGCCTGCCTCG

Phenotype

MIM: 610334 MIM: 610385

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

TMEM176A PubMed Links

Gene Details

Gene

TMEM176A

Gene Name

transmembrane protein 176A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018487.2	384	Silent Mutation	TCA,TCG	S57S	NP_060957.2
XM_011516376.2	384	Silent Mutation	TCA,TCG	S74S	XP_011514678.1
XM_011516377.2	384	Silent Mutation	TCA,TCG	S74S	XP_011514679.1
XM_011516378.2	384	Silent Mutation	TCA,TCG	S74S	XP_011514680.1
XM_017012393.1	384	Silent Mutation	TCA,TCG	S57S	XP_016867882.1

Gene

TMEM176B

Gene Name

transmembrane protein 176B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001101311.1	384	Intron			NP_001094781.1
NM_001101312.1	384	Intron			NP_001094782.1
NM_001101314.1	384	Intron			NP_001094784.1
NM_014020.3	384	Intron			NP_054739.3
XM_006715933.3	384	Intron			XP_006715996.2

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