Product Details

SNP ID
rs199808769
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:140632399 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTCAGACAGGTCTAGGCTGGTAAG[G/T]GCCGGGAAGGCGCGAACCTGTTCGC
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_000591.3 977 Silent Mutation GCA,GCC A195A NP_000582.1
NM_001040021.2 977 Silent Mutation GCA,GCC A195A NP_001035110.1
NM_001174104.1 977 Silent Mutation GCA,GCC A195A NP_001167575.1
NM_001174105.1 977 Silent Mutation GCA,GCC A195A 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_001300980.1 977 Intron NP_001287909.1
NM_001300982.1 977 Intron NP_001287911.1
NM_018502.4 977 Intron NP_060972.3
XM_005268477.1 977 Intron XP_005268534.1
XM_011537663.2 977 Intron XP_011535965.1
XM_011537665.2 977 Intron XP_011535967.1
XM_011537668.2 977 Intron XP_011535970.1
XM_017009617.1 977 Intron XP_016865106.1
XM_017009618.1 977 Intron XP_016865107.1
XM_017009619.1 977 Intron XP_016865108.1
XM_017009620.1 977 Intron XP_016865109.1

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