Product Details

SNP ID
rs6739976
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:42343285 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AGGATAACTGCAGAATTCCTCAATA[A/C]CAAGGCCGTTTGCTAGCCATGTGGT
Phenotype
MIM: 605771
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
COX7A2L PubMed Links

Gene Details

Gene
COX7A2L
Gene Name
cytochrome c oxidase subunit 7A2 like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001319036.1 Intron NP_001305965.1
NM_001319037.1 Intron NP_001305966.1
NM_001319038.1 Intron NP_001305967.1
NM_001319040.1 Intron NP_001305969.1
NM_004718.3 Intron NP_004709.2

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