Product Details

SNP ID

rs6536991

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:140560427 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATCCTTCACTCCCAAAACATGTCTT[C/T]TCTTCACTGACATGAACTTTTTCAA

Phenotype

MIM: 610196 MIM: 113730

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

ELMOD2 PubMed Links

Additional Information

For this assay, SNP(s) [rs78724285] are located under a primer 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

ELMOD2

Gene Name

ELMO domain containing 2

There are no transcripts associated with this gene.

Gene

UCP1

Gene Name

uncoupling protein 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_021833.4	1312	Intron			NP_068605.1
XM_005263206.3	1312	Intron			XP_005263263.1
XM_011532228.2	1312	UTR 3			XP_011530530.1

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