Product Details

SNP ID
rs142187685
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:43446451 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAACATCCAGGGAAGAAAGCACCAT[A/G]AGTCTTTGAGCTTGAAAAGGTGCAT
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 1802 Missense Mutation TCA,TTA S140L NP_071928.2
XM_005248333.4 1802 Missense Mutation TCA,TTA S140L XP_005248390.1
XM_005248335.3 1802 Missense Mutation TCA,TTA S140L XP_005248392.1
XM_006714486.3 1802 Missense Mutation TCA,TTA S140L XP_006714549.1
XM_011514074.2 1802 Missense Mutation TCA,TTA S140L XP_011512376.1
XM_011514075.2 1802 Missense Mutation TCA,TTA S140L XP_011512377.1

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