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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