Product Details

SNP ID

rs12069017

Assay Type

Functionally tested

NCBI dbSNP Submissions

1

Location

Chr.1:10947730 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAGCTCAGGAGGCCTGTGGCTTTCA[A/G]CACTGAGGGCCAAGGTGGGCTCTGT

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	2323	Missense Mutation	GCT,GTT	A802V	NP_001164225.1
XM_017000373.1	2323	Missense Mutation	GCT,GTT	A766V	XP_016855862.1

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