Product Details

SNP ID
rs140017853
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:61562336 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGGTGGATTTTGTTCCTGAAAATC[A/G]CCAGTTCCGTGCTCCATTATGTCGT
Phenotype
MIM: 176886
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
PTPRG PubMed Links

Gene Details

Gene
PTPRG
Gene Name
protein tyrosine phosphatase, receptor type G
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_002841.3 426 Missense Mutation ACC,GCC T17A NP_002832.3
XM_005265353.3 426 Missense Mutation ACC,GCC T17A XP_005265410.1
XM_017006961.1 426 Missense Mutation ACC,GCC T17A XP_016862450.1
XM_017006962.1 426 Intron XP_016862451.1
XM_017006963.1 426 Missense Mutation ACC,GCC T17A XP_016862452.1
XM_017006964.1 426 Intron XP_016862453.1

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