Product Details

SNP ID
rs4661079
Assay Type
Functionally tested
NCBI dbSNP Submissions
48
Location
Chr.1:156013507 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CAATATGAACTGAAGGCAGAAAACA[A/G]GGAGACATAGCTCAAAGCTGGGTCT
Phenotype
MIM: 600867
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SSR2 PubMed Links

Gene Details

Gene
SSR2
Gene Name
signal sequence receptor subunit 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_003145.3 Intron NP_003136.1
XM_011509923.2 Intron XP_011508225.1

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