Product Details
- SNP ID
-
rs16828251
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:231592982 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- ACTCCCAGGGTACCCCCTGGGCAAC[C/G]TGGATGACAGCAGGTCTAAGGACAG
- Phenotype
-
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
C2orf57
PubMed Links
Gene Details
- Gene
- C2orf57
- Gene Name
- chromosome 2 open reading frame 57
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_152614.2 |
119 |
Missense Mutation |
CTG,GTG |
L11V |
NP_689827.2 |
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