Product Details

SNP ID

rs140770075

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:150802274 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCTAGGAGGATTTTTCTACATCCG[C/T]GACTACACCCTCCTCGTCACCTCGG

Phenotype

MIM: 610334 MIM: 610385

Polymorphism

C/T, 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	447	Silent Mutation	CGC,CGT	R78R	NP_060957.2
XM_011516376.2	447	Silent Mutation	CGC,CGT	R95R	XP_011514678.1
XM_011516377.2	447	Silent Mutation	CGC,CGT	R95R	XP_011514679.1
XM_011516378.2	447	Silent Mutation	CGC,CGT	R95R	XP_011514680.1
XM_017012393.1	447	Silent Mutation	CGC,CGT	R78R	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	447	Intron			NP_001094781.1
NM_001101312.1	447	Intron			NP_001094782.1
NM_001101314.1	447	Intron			NP_001094784.1
NM_014020.3	447	Intron			NP_054739.3
XM_006715933.3	447	Intron			XP_006715996.2

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