Product Details

SNP ID
rs149594885
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:45652163 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCGAGGCCGTGAGCTTGAAGCCCAC[A/G]GCCTGGTCGCTGCGCCATGCGGTGG
Phenotype
MIM: 176975
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
LOC102724965 PubMed Links

Gene Details

Gene
LOC102724965
Gene Name
collagen alpha-2(I) chain-like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
XM_011533229.2 849 Intron XP_011531531.2
Gene
PRKCE
Gene Name
protein kinase C epsilon
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_005400.2 849 Silent Mutation ACA,ACG T21T NP_005391.1
XM_005264428.1 849 Silent Mutation ACA,ACG T21T XP_005264485.1
XM_005264431.3 849 Silent Mutation ACA,ACG T21T XP_005264488.1
XM_006712050.3 849 Intron XP_006712113.1
XM_011532971.2 849 Intron XP_011531273.1
XM_011532975.2 849 Intron XP_011531277.1
XM_011532978.1 849 Intron XP_011531280.1
XM_011532980.2 849 Intron XP_011531282.1
XM_011532981.2 849 Intron XP_011531283.1
XM_011532982.1 849 Intron XP_011531284.1
XM_011532983.2 849 Intron XP_011531285.1
XM_017004486.1 849 Intron XP_016859975.1
XM_017004487.1 849 Intron XP_016859976.1
XM_017004488.1 849 Intron XP_016859977.1
XM_017004489.1 849 Intron XP_016859978.1
XM_017004490.1 849 Intron XP_016859979.1
XM_017004491.1 849 Intron XP_016859980.1
XM_017004492.1 849 Silent Mutation ACA,ACG T21T XP_016859981.1

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