Product Details

SNP ID
rs199928598
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:140632255 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGGCTGCACACCTGCCGCCGCCAG[G/T]GCGGCGCACACGCCTGTGGGCGTCT
Phenotype
MIM: 158120
Polymorphism
G/T, Transversion 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 1121 Silent Mutation NP_000582.1
NM_001040021.2 1121 Silent Mutation NP_001035110.1
NM_001174104.1 1121 Silent Mutation NP_001167575.1
NM_001174105.1 1121 Silent 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 1121 Intron NP_001287909.1
NM_001300982.1 1121 Intron NP_001287911.1
NM_018502.4 1121 Intron NP_060972.3
XM_005268477.1 1121 Intron XP_005268534.1
XM_011537663.2 1121 Intron XP_011535965.1
XM_011537665.2 1121 Intron XP_011535967.1
XM_011537668.2 1121 Intron XP_011535970.1
XM_017009617.1 1121 Intron XP_016865106.1
XM_017009618.1 1121 Intron XP_016865107.1
XM_017009619.1 1121 Intron XP_016865108.1
XM_017009620.1 1121 Intron XP_016865109.1

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