Product Details

SNP ID
rs3806556
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:218660284 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GTATTGTAGAGAGCCTTGAGTACCA[A/G]GCTGAGTTTATACCCAATTCAGGGG
Phenotype
MIM: 603647 MIM: 616014 MIM: 604083
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
BCS1L PubMed Links
Additional Information
For this assay, SNP(s) [rs77595651] 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
BCS1L
Gene Name
BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001079866.1 333 Intron NP_001073335.1
NM_001257342.1 333 Intron NP_001244271.1
NM_001257343.1 333 Intron NP_001244272.1
NM_001257344.1 333 Intron NP_001244273.1
NM_001318836.1 333 Intron NP_001305765.1
NM_001320717.1 333 Intron NP_001307646.1
NM_004328.4 333 Intron NP_004319.1
XM_005246748.2 333 UTR 5 XP_005246805.1
XM_005246749.3 333 Intron XP_005246806.1
XM_006712678.1 333 UTR 5 XP_006712741.1
XM_017004631.1 333 UTR 5 XP_016860120.1
XM_017004632.1 333 Intron XP_016860121.1
XM_017004633.1 333 UTR 5 XP_016860122.1
XM_017004634.1 333 Intron XP_016860123.1
Gene
RNF25
Gene Name
ring finger protein 25
There are no transcripts associated with this gene.

Gene
ZNF142
Gene Name
zinc finger protein 142
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001105537.2 333 Intron NP_001099007.1
XM_006712730.3 333 Intron XP_006712793.1
XM_011511784.2 333 Intron XP_011510086.1
XM_011511785.2 333 Intron XP_011510087.1
XM_011511786.2 333 Intron XP_011510088.1
XM_011511787.2 333 Intron XP_011510089.1
XM_011511788.2 333 Intron XP_011510090.1
XM_011511789.2 333 Intron XP_011510091.1
XM_017004871.1 333 Intron XP_016860360.1
XM_017004872.1 333 Intron XP_016860361.1

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