Product Details

SNP ID
rs139519201
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.19:5208047 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCGTGATGAAGACGCCCGTCCTGC[C/T]CACGCCGGCACTGGTGGCAGTAAAG
Phenotype
MIM: 601576
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
PTPRS PubMed Links

Gene Details

Gene
PTPRS
Gene Name
protein tyrosine phosphatase, receptor type S
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_002850.3 5816 Missense Mutation AGC,GGC S1885G NP_002841.3
NM_130853.2 5816 Missense Mutation AGC,GGC S1438G NP_570923.2
NM_130854.2 5816 Missense Mutation AGC,GGC S1847G NP_570924.2
NM_130855.2 5816 Missense Mutation AGC,GGC S1442G NP_570925.2
XM_005259600.2 5816 Missense Mutation AGC,GGC S1872G XP_005259657.1
XM_005259606.2 5816 Missense Mutation AGC,GGC S1847G XP_005259663.1
XM_005259607.2 5816 Missense Mutation AGC,GGC S1843G XP_005259664.1
XM_005259609.1 5816 Missense Mutation AGC,GGC S1438G XP_005259666.1
XM_005259610.1 5816 Missense Mutation AGC,GGC S1434G XP_005259667.1
XM_011528157.2 5816 Missense Mutation AGC,GGC S1454G XP_011526459.1
XM_011528158.2 5816 Missense Mutation AGC,GGC S1094G XP_011526460.1
XM_017027065.1 5816 Missense Mutation AGC,GGC S1876G XP_016882554.1
XM_017027066.1 5816 Missense Mutation AGC,GGC S1876G XP_016882555.1
XM_017027067.1 5816 Missense Mutation AGC,GGC S1876G XP_016882556.1
XM_017027068.1 5816 Missense Mutation AGC,GGC S1872G XP_016882557.1
XM_017027069.1 5816 Missense Mutation AGC,GGC S1867G XP_016882558.1
XM_017027070.1 5816 Missense Mutation AGC,GGC S1860G XP_016882559.1
XM_017027071.1 5816 Missense Mutation AGC,GGC S1856G XP_016882560.1
XM_017027072.1 5816 Missense Mutation AGC,GGC S1847G XP_016882561.1
XM_017027073.1 5816 Missense Mutation AGC,GGC S1634G XP_016882562.1
XM_017027074.1 5816 Missense Mutation AGC,GGC S1458G XP_016882563.1
XM_017027075.1 5816 Missense Mutation AGC,GGC S1454G XP_016882564.1
XM_017027076.1 5816 Missense Mutation AGC,GGC S1442G XP_016882565.1

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