Product Details

SNP ID
rs3211097
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:227329764 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TATTTAAATGAGTAAAGGAACAAGC[A/T]GTGACACATCACTAGGAAGGTCAGT
Phenotype
MIM: 614785
Polymorphism
A/T, Transversion Substitution
Allele Nomenclature
Literature Links
LOC654841 PubMed Links
Additional Information
For this assay, SNP(s) [rs3211098] 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
LOC654841
Gene Name
uncharacterized LOC654841
There are no transcripts associated with this gene.

Gene
MFF
Gene Name
mitochondrial fission factor
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001277061.1 532 Intron NP_001263990.1
NM_001277062.1 532 Intron NP_001263991.1
NM_001277063.1 532 Intron NP_001263992.1
NM_001277064.1 532 Intron NP_001263993.1
NM_001277065.1 532 Intron NP_001263994.1
NM_001277066.1 532 Intron NP_001263995.1
NM_001277067.1 532 Intron NP_001263996.1
NM_001277068.1 532 Intron NP_001263997.1
NM_020194.5 532 Intron NP_064579.3
XM_005246681.3 532 Intron XP_005246738.1
XM_005246682.1 532 Intron XP_005246739.1
XM_005246683.1 532 Intron XP_005246740.1
XM_005246684.1 532 Intron XP_005246741.1
XM_005246685.3 532 Intron XP_005246742.1
XM_005246686.3 532 Intron XP_005246743.1
XM_005246687.3 532 Intron XP_005246744.1
XM_005246688.1 532 Intron XP_005246745.1
XM_006712637.1 532 Intron XP_006712700.1
XM_006712638.1 532 Intron XP_006712701.1
XM_006712639.2 532 Intron XP_006712702.1
XM_011511500.1 532 Intron XP_011509802.1
XM_011511501.1 532 Intron XP_011509803.1
XM_017004512.1 532 Missense Mutation AGT,TGT S7C XP_016860001.1
XM_017004513.1 532 Intron XP_016860002.1
XM_017004514.1 532 Intron XP_016860003.1
XM_017004515.1 532 Intron XP_016860004.1

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