Product Details

SNP ID

rs4914

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:140631883 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGGCAAAGCCCCGGGCCCCTTGGAG[C/G]AGCACCAGGGTTCCCGACACCCCCA

Phenotype

MIM: 158120

Polymorphism

C/G, 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	1493	Silent Mutation	CTC,CTG	L367L	NP_000582.1
NM_001040021.2	1493	Silent Mutation	CTC,CTG	L367L	NP_001035110.1
NM_001174104.1	1493	Silent Mutation	CTC,CTG	L367L	NP_001167575.1
NM_001174105.1	1493	Silent Mutation	CTC,CTG	L367L	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	1493	Intron			NP_001287909.1
NM_001300982.1	1493	Intron			NP_001287911.1
NM_018502.4	1493	Intron			NP_060972.3
XM_005268477.1	1493	Intron			XP_005268534.1
XM_011537663.2	1493	Intron			XP_011535965.1
XM_011537665.2	1493	Intron			XP_011535967.1
XM_011537668.2	1493	Intron			XP_011535970.1
XM_017009617.1	1493	Intron			XP_016865106.1
XM_017009618.1	1493	Intron			XP_016865107.1
XM_017009619.1	1493	Intron			XP_016865108.1
XM_017009620.1	1493	Intron			XP_016865109.1

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