Product Details

SNP ID

hCV60119913

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:65196253 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAAATAAATAAGTTATTTACATTTC[A/C]AGTAAAAGTATTGTGTTTTATTTCT

Phenotype

MIM: 603489

Polymorphism

A/C, Transversion 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	4214	UTR 3			NP_003604.3

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