Product Details

SNP ID

rs150705129

Assay Type

Functionally tested

NCBI dbSNP Submissions

4

Location

Chr.1:10947862 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGAGCCCACAGGCTCAGGGTTTGC[A/G]TGGATGGAGGGCTGGACGTGTGTGC

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

C1orf127 PubMed Links

Gene Details

Gene

C1orf127

Gene Name

chromosome 1 open reading frame 127

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001170754.1	2191	Missense Mutation	ACG,ATG	T758M	NP_001164225.1
XM_017000373.1	2191	Missense Mutation	ACG,ATG	T722M	XP_016855862.1

View Full Product Details