Product Details

SNP ID
rs143301490
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:112767561 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAGCTGTGGCGGGTCAGCTTCTTCA[A/G]TATCTACTGTTTTTATCAACTCTGC
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
TMEM168 PubMed Links

Gene Details

Gene
TMEM168
Gene Name
transmembrane protein 168
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001287497.1 2122 Missense Mutation ACT,ATT T577I NP_001274426.1
NM_022484.5 2122 Missense Mutation ACT,ATT T577I NP_071929.3
XM_017012523.1 2122 Missense Mutation ACT,ATT T577I XP_016868012.1
XM_017012524.1 2122 Intron XP_016868013.1
XM_017012525.1 2122 Missense Mutation ACT,ATT T193I XP_016868014.1

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