Product Details

SNP ID

rs12119716

Assay Type

Functionally Tested

NCBI dbSNP Submissions

13

Location

Chr.1:11988614 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCAGTGGACTGATCATAGGTCACT[A/G]CAGCCGAAACTCCTGGGCTCAAGTG

Phenotype

MIM: 608507

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

MFN2 PubMed Links

Additional Information

For this assay, SNP(s) [rs116980326] 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

MFN2

Gene Name

mitofusin 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001127660.1		Intron			NP_001121132.1
NM_014874.3		Intron			NP_055689.1
XM_005263543.3		Intron			XP_005263600.1
XM_005263545.3		Intron			XP_005263602.1
XM_005263547.3		Intron			XP_005263604.1
XM_005263548.3		Intron			XP_005263605.1

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