Product Details

SNP ID
rs35519567
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:23246906 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGATTTCTGCTCCTGGCTGCAAGA[C/T]TGCCACTTGATGCCGCCAAACGTGA
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_001005340.1 701 Silent Mutation CTG,TTG L17L NP_001005340.1
NM_002510.2 701 Silent Mutation CTG,TTG L17L NP_002501.1
XM_005249578.2 701 Silent Mutation CTG,TTG L17L XP_005249635.1
XM_017011676.1 701 Silent Mutation CTG,TTG L17L XP_016867165.1
XM_017011677.1 701 Silent Mutation CTG,TTG L17L XP_016867166.1
XM_017011678.1 701 Silent Mutation CTG,TTG L17L XP_016867167.1
Gene
LOC101927890
Gene Name
uncharacterized LOC101927890
There are no transcripts associated with this gene.

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