Product Details

SNP ID
rs17147950
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:23250965 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTTTCATATGACTCAAGTGAATTTC[C/T]AATTACAAATACTTATTGATAAACA
Phenotype
MIM: 604368
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
GPNMB PubMed Links

Gene Details

Gene
GPNMB
Gene Name
glycoprotein nmb
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001005340.1 Intron NP_001005340.1
NM_002510.2 Intron NP_002501.1
XM_005249578.2 Intron XP_005249635.1
XM_017011676.1 Intron XP_016867165.1
XM_017011677.1 Intron XP_016867166.1
XM_017011678.1 Intron XP_016867167.1

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