Product Details

SNP ID
rs61757813
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:157540717 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGAGGCCCCTGAGGCTGCCGCTCA[A/C]TGGGGAAGGGCCTTGAGGATGGCGT
Phenotype
MIM: 601698
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
PTPRN2 PubMed Links

Gene Details

Gene
PTPRN2
Gene Name
protein tyrosine phosphatase, receptor type N2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001308267.1 3178 Silent Mutation NP_001295196.1
NM_001308268.1 3178 Silent Mutation NP_001295197.1
NM_002847.4 3178 Silent Mutation NP_002838.2
NM_130842.3 3178 Silent Mutation NP_570857.2
NM_130843.3 3178 Silent Mutation NP_570858.2
XM_011516446.1 3178 Intron XP_011514748.1
XM_011516447.2 3178 Intron XP_011514749.1
XM_011516448.2 3178 Intron XP_011514750.1
XM_011516449.2 3178 Intron XP_011514751.1
XM_017012475.1 3178 Missense Mutation XP_016867964.1
XM_017012476.1 3178 Intron XP_016867965.1

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