Product Details

SNP ID
rs11556179
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.5:140631963 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ACCACGCCGGAGTTCATTGAGCCCT[C/T]GTGGGGGAGGGCAGTTCCAGGGACC
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 1413 Missense Mutation AAG,GAG K341E NP_000582.1
NM_001040021.2 1413 Missense Mutation AAG,GAG K341E NP_001035110.1
NM_001174104.1 1413 Missense Mutation AAG,GAG K341E NP_001167575.1
NM_001174105.1 1413 Missense Mutation AAG,GAG K341E 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 1413 Intron NP_001287909.1
NM_001300982.1 1413 Intron NP_001287911.1
NM_018502.4 1413 Intron NP_060972.3
XM_005268477.1 1413 Intron XP_005268534.1
XM_011537663.2 1413 Intron XP_011535965.1
XM_011537665.2 1413 Intron XP_011535967.1
XM_011537668.2 1413 Intron XP_011535970.1
XM_017009617.1 1413 Intron XP_016865106.1
XM_017009618.1 1413 Intron XP_016865107.1
XM_017009619.1 1413 Intron XP_016865108.1
XM_017009620.1 1413 Intron XP_016865109.1

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