Product Details

SNP ID
rs2067864
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.2:62454034 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GGGCCTGTTTTCTAGAAGGAACTCT[C/T]TTACTTAAAGGAAAGCTTCAGGATG
Phenotype
MIM: 614950
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
TMEM17 PubMed Links

Gene Details

Gene
TMEM17
Gene Name
transmembrane protein 17
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_198276.2 Intron NP_938017.2
XM_011532693.2 Intron XP_011530995.1
XM_011532694.2 Intron XP_011530996.1
XM_017003575.1 Intron XP_016859064.1

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