Product Details

SNP ID

rs138915136

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:240126620 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTTCCCTTCTTCTCCACCAGCAAC[A/G]GATGGTGTTTCATCACTCTTAAAAC

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

COPS9 PubMed Links

Gene Details

Gene

COPS9

Gene Name

COP9 signalosome subunit 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001163424.1	1127	Intron			NP_001156896.1
NM_138336.1	1127	Silent Mutation			NP_612209.1
XM_017003411.1	1127	Silent Mutation			XP_016858900.1

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