Product Details

SNP ID

rs192398187

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:43446541 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGAACAGTGAAGGAAAGGTCTTCGC[A/G]GGAGAGTCAAAGCAGCCTGAGGGAG

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

TMEM267 PubMed Links

Gene Details

Gene

TMEM267

Gene Name

transmembrane protein 267

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_022483.4	1712	Missense Mutation	CCG,CTG	P110L	NP_071928.2
XM_005248333.4	1712	Missense Mutation	CCG,CTG	P110L	XP_005248390.1
XM_005248335.3	1712	Missense Mutation	CCG,CTG	P110L	XP_005248392.1
XM_006714486.3	1712	Missense Mutation	CCG,CTG	P110L	XP_006714549.1
XM_011514074.2	1712	Missense Mutation	CCG,CTG	P110L	XP_011512376.1
XM_011514075.2	1712	Missense Mutation	CCG,CTG	P110L	XP_011512377.1

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