Product Details

SNP ID

rs201228241

Assay Type

Functionally tested

NCBI dbSNP Submissions

3

Location

Chr.1:1084503 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TACGGCTTCGCCAGGCTGCAGGGCC[A/G]GAGCTGTGGGGGAGAAAGCGGAGAG

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

C1orf159 PubMed Links

Gene Details

Gene

C1orf159

Gene Name

chromosome 1 open reading frame 159

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_017891.4	847	Missense Mutation	CCG,CTG	P150L	NP_060361.4
XM_005244765.2	847	Missense Mutation	CCG,CTG	P150L	XP_005244822.1
XM_006710717.2	847	Missense Mutation	CCG,CTG	P150L	XP_006710780.1
XM_006710718.2	847	Missense Mutation	CCG,CTG	P150L	XP_006710781.1
XM_011541651.2	847	Missense Mutation	CCG,CTG	P218L	XP_011539953.1
XM_011541652.2	847	Missense Mutation	CCG,CTG	P218L	XP_011539954.1
XM_011541653.2	847	Missense Mutation	CCG,CTG	P218L	XP_011539955.1
XM_011541655.2	847	Missense Mutation	CCG,CTG	P218L	XP_011539957.1
XM_011541656.2	847	Missense Mutation	CCG,CTG	P218L	XP_011539958.1
XM_011541658.2	847	Missense Mutation	CCG,CTG	P218L	XP_011539960.1
XM_011541659.2	847	Missense Mutation	CCG,CTG	P218L	XP_011539961.1
XM_011541660.2	847	Missense Mutation	CCG,CTG	P218L	XP_011539962.1
XM_011541661.2	847	Missense Mutation	CCG,CTG	P186L	XP_011539963.1
XM_011541662.2	847	Missense Mutation	CCG,CTG	P186L	XP_011539964.1
XM_011541663.2	847	Missense Mutation	CCG,CTG	P186L	XP_011539965.1
XM_011541665.2	847	Missense Mutation	CCG,CTG	P150L	XP_011539967.1
XM_017001572.1	847	Missense Mutation	CCG,CTG	P218L	XP_016857061.1
XM_017001573.1	847	Missense Mutation	CCG,CTG	P218L	XP_016857062.1
XM_017001574.1	847	Missense Mutation	CCG,CTG	P218L	XP_016857063.1
XM_017001575.1	847	Missense Mutation	CCG,CTG	P218L	XP_016857064.1
XM_017001576.1	847	Missense Mutation	CCG,CTG	P186L	XP_016857065.1
XM_017001577.1	847	Missense Mutation	CCG,CTG	P150L	XP_016857066.1
XM_017001578.1	847	Missense Mutation	CCG,CTG	P150L	XP_016857067.1
XM_017001579.1	847	Missense Mutation	CCG,CTG	P150L	XP_016857068.1
XM_017001580.1	847	Missense Mutation	CCG,CTG	P218L	XP_016857069.1

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