Product Details

SNP ID
rs79813353
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:60422626 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTCAGATGGGCAAGGGGGTGAAGGG[A/G]ACAAGCCACTAGAGCAGGTGAAGTG
Phenotype
MIM: 607740
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
C17orf64 PubMed Links

Gene Details

Gene
C17orf64
Gene Name
chromosome 17 open reading frame 64
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_181707.2 125 Missense Mutation AAC,GAC N12D NP_859058.2
XM_005257033.4 125 Intron XP_005257090.1
XM_005257034.4 125 Intron XP_005257091.1
XM_005257035.4 125 Intron XP_005257092.1
XM_005257036.2 125 Missense Mutation AAC,GAC N12D XP_005257093.1
XM_017024166.1 125 Intron XP_016879655.1
Gene
USP32
Gene Name
ubiquitin specific peptidase 32
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_032582.3 125 Intron NP_115971.2
XM_011525371.1 125 Intron XP_011523673.1
XM_011525372.1 125 Intron XP_011523674.1
XM_011525373.1 125 Intron XP_011523675.1
XM_011525374.1 125 Intron XP_011523676.1
XM_011525375.1 125 Intron XP_011523677.1
XM_011525376.1 125 Intron XP_011523678.1
XM_011525378.1 125 Intron XP_011523680.1
XM_011525379.2 125 Intron XP_011523681.1
XM_017025233.1 125 Intron XP_016880722.1
XM_017025234.1 125 Intron XP_016880723.1

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