Product Details

SNP ID
rs200391671
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:140632497 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTGGCTTGAGCCACTGCTGCAGCT[C/T]GGCGAGCCAAGAACGCCCTGTCGCC
Phenotype
MIM: 158120
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CD14 PubMed Links

Gene Details

Gene
CD14
Gene Name
CD14 molecule
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000591.3 879 Missense Mutation NP_000582.1
NM_001040021.2 879 Missense Mutation NP_001035110.1
NM_001174104.1 879 Missense Mutation NP_001167575.1
NM_001174105.1 879 Missense Mutation NP_001167576.1
Gene
TMCO6
Gene Name
transmembrane and coiled-coil domains 6
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001300980.1 879 Intron NP_001287909.1
NM_001300982.1 879 Intron NP_001287911.1
NM_018502.4 879 Intron NP_060972.3
XM_005268477.1 879 Intron XP_005268534.1
XM_011537663.2 879 Intron XP_011535965.1
XM_011537665.2 879 Intron XP_011535967.1
XM_011537668.2 879 Intron XP_011535970.1
XM_017009617.1 879 Intron XP_016865106.1
XM_017009618.1 879 Intron XP_016865107.1
XM_017009619.1 879 Intron XP_016865108.1
XM_017009620.1 879 Intron XP_016865109.1

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