Product Details

SNP ID
rs8078984
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:48835189 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AGGAATTTTATCACTGGGAGGAAGG[A/G]AAGACTAAAGATTACTGACCTGAAA
Phenotype
MIM: 604587
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CALCOCO2 PubMed Links

Gene Details

Gene
CALCOCO2
Gene Name
calcium binding and coiled-coil domain 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001261390.1 Intron NP_001248319.1
NM_001261391.1 Intron NP_001248320.1
NM_001261393.1 Intron NP_001248322.1
NM_001261395.1 Intron NP_001248324.1
NM_005831.4 Intron NP_005822.1

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