Product Details

SNP ID
rs938952
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:65196790 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AATCTCAGAGAGGCCACCACTCCAC[C/T]CTGGCGCTGGCCACCCCTGCTCGCT
Phenotype
MIM: 603489
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CILP PubMed Links

Gene Details

Gene
CILP
Gene Name
cartilage intermediate layer protein
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_003613.3 3677 Missense Mutation AGT,GGT S1166G NP_003604.3
XM_017022678.1 3677 Missense Mutation AGT,GGT S1193G XP_016878167.1
XM_017022679.1 3677 Missense Mutation AGT,GGT S1142G XP_016878168.1

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