Product Details

SNP ID
rs201779058
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:23246862 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGCGTCCGTGAGAATTCAGCATGG[A/G]ATGTCTCTACTATTTCCTGGGATTT
Phenotype
MIM: 604368
Polymorphism
A/G, 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_001005340.1 657 Missense Mutation GAA,GGA E2G NP_001005340.1
NM_002510.2 657 Missense Mutation GAA,GGA E2G NP_002501.1
XM_005249578.2 657 Missense Mutation GAA,GGA E2G XP_005249635.1
XM_017011676.1 657 Missense Mutation GAA,GGA E2G XP_016867165.1
XM_017011677.1 657 Missense Mutation GAA,GGA E2G XP_016867166.1
XM_017011678.1 657 Missense Mutation GAA,GGA E2G XP_016867167.1
Gene
LOC101927890
Gene Name
uncharacterized LOC101927890
There are no transcripts associated with this gene.

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