Product Details

SNP ID
rs142926929
Assay Type
Functionally tested
NCBI dbSNP Submissions
16
Location
Chr.1:9596947 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCGCGCCCAGCCTGCGCGACCCTT[C/T]GCAGCCGCAGCAGTGGGTGAGCAGC
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
TMEM201 PubMed Links

Gene Details

Gene
TMEM201
Gene Name
transmembrane protein 201
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001010866.3 380 Missense Mutation TCG,TTG S108L NP_001010866.1
NM_001130924.2 380 Missense Mutation TCG,TTG S108L NP_001124396.2
XM_006710417.3 380 Missense Mutation TCG,TTG S108L XP_006710480.1
XM_011540910.2 380 Missense Mutation TCG,TTG S108L XP_011539212.1
XM_017000549.1 380 Missense Mutation TCG,TTG S108L XP_016856038.1
XM_017000550.1 380 Missense Mutation TCG,TTG S108L XP_016856039.1
XM_017000551.1 380 Missense Mutation TCG,TTG S70L XP_016856040.1
XM_017000552.1 380 Missense Mutation TCG,TTG S70L XP_016856041.1

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