Product Details

SNP ID

rs200033604

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.2:97757390 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGTGTTACCGAGGACCGACTGCGA[C/G]AAAACAGAAAGCGTCCAGCACTGAG

Phenotype

MIM: 615659

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

TMEM131 PubMed Links

Additional Information

For this assay, SNP(s) [rs115906722] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

TMEM131

Gene Name

transmembrane protein 131

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015348.1		Intron			NP_056163.1
XM_005263909.1		Intron			XP_005263966.1
XM_005263910.1		Intron			XP_005263967.1
XM_005263911.1		Intron			XP_005263968.1
XM_005263912.3		Intron			XP_005263969.1
XM_011510869.1		Intron			XP_011509171.1

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