Product Details

SNP ID

rs6668699

Assay Type

Functionally tested

NCBI dbSNP Submissions

40

Location

Chr.1:11766573 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAGGTGCCAGGCTCCCCAGGAACCC[C/T]CCGGTGCTGTGCAGCAGGACCTCTG

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

C1orf167 PubMed Links

Gene Details

Gene

C1orf167

Gene Name

chromosome 1 open reading frame 167

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001010881.1	1084	Missense Mutation	CCC,TCC	P263S	NP_001010881.1
XM_011541269.2	1084	Missense Mutation	CCC,TCC	P308S	XP_011539571.2
XM_011541271.2	1084	Missense Mutation	CCC,TCC	P308S	XP_011539573.2
XM_011541272.2	1084	Missense Mutation	CCC,TCC	P308S	XP_011539574.1
XM_011541274.2	1084	Missense Mutation	CCC,TCC	P263S	XP_011539576.2
XM_011541275.2	1084	Missense Mutation	CCC,TCC	P263S	XP_011539577.2
XM_011541276.2	1084	Missense Mutation	CCC,TCC	P308S	XP_011539578.1
XM_011541277.2	1084	Missense Mutation	CCC,TCC	P308S	XP_011539579.1
XM_011541278.2	1084	Missense Mutation	CCC,TCC	P308S	XP_011539580.1
XM_011541280.2	1084	Intron			XP_011539582.2
XM_011541281.2	1084	Intron			XP_011539583.2
XM_017001062.1	1084	Missense Mutation	CCC,TCC	P308S	XP_016856551.1
XM_017001063.1	1084	Missense Mutation	CCC,TCC	P308S	XP_016856552.1
XM_017001064.1	1084	Missense Mutation	CCC,TCC	P308S	XP_016856553.1

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