Product Details

SNP ID

rs2271018

Assay Type

Functionally tested

NCBI dbSNP Submissions

50

Location

Chr.1:200898364 on Build GRCh38

Set Membership

HapMap JSNP

Context Sequence [VIC/FAM]

GCCCAGGCTGGTCACGGTGTCCCCC[C/G]TCCCTGCTCTGTGCCCTCTCCTTCC

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

C1orf106 PubMed Links

Gene Details

Gene

C1orf106

Gene Name

chromosome 1 open reading frame 106

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001142569.2	325	UTR 5			NP_001136041.1
NM_018265.3	325	Silent Mutation	CCC,CCG	P87P	NP_060735.3
XM_011509754.2	325	Intron			XP_011508056.1
XM_011509755.1	325	Intron			XP_011508057.1
XM_011509756.2	325	Silent Mutation	CCC,CCG	P87P	XP_011508058.1

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