Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGCGTGATGAAGACGCCCGTCCTGC[C/T]CACGCCGGCACTGGTGGCAGTAAAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601576 | ||||||||||||||||||||
Literature Links: |
PTPRS PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
PTPRS - protein tyrosine phosphatase, receptor type S | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002850.3 | 5816 | Missense Mutation | AGC,GGC | S,G 1885 | NP_002841.3 | |
NM_130853.2 | 5816 | Missense Mutation | AGC,GGC | S,G 1438 | NP_570923.2 | |
NM_130854.2 | 5816 | Missense Mutation | AGC,GGC | S,G 1847 | NP_570924.2 | |
NM_130855.2 | 5816 | Missense Mutation | AGC,GGC | S,G 1442 | NP_570925.2 | |
XM_005259600.2 | 5816 | Missense Mutation | AGC,GGC | S,G 1872 | XP_005259657.1 | |
XM_005259606.2 | 5816 | Missense Mutation | AGC,GGC | S,G 1847 | XP_005259663.1 | |
XM_005259607.2 | 5816 | Missense Mutation | AGC,GGC | S,G 1843 | XP_005259664.1 | |
XM_005259609.1 | 5816 | Missense Mutation | AGC,GGC | S,G 1438 | XP_005259666.1 | |
XM_005259610.1 | 5816 | Missense Mutation | AGC,GGC | S,G 1434 | XP_005259667.1 | |
XM_011528157.2 | 5816 | Missense Mutation | AGC,GGC | S,G 1454 | XP_011526459.1 | |
XM_011528158.2 | 5816 | Missense Mutation | AGC,GGC | S,G 1094 | XP_011526460.1 | |
XM_017027065.1 | 5816 | Missense Mutation | AGC,GGC | S,G 1876 | XP_016882554.1 | |
XM_017027066.1 | 5816 | Missense Mutation | AGC,GGC | S,G 1876 | XP_016882555.1 | |
XM_017027067.1 | 5816 | Missense Mutation | AGC,GGC | S,G 1876 | XP_016882556.1 | |
XM_017027068.1 | 5816 | Missense Mutation | AGC,GGC | S,G 1872 | XP_016882557.1 | |
XM_017027069.1 | 5816 | Missense Mutation | AGC,GGC | S,G 1867 | XP_016882558.1 | |
XM_017027070.1 | 5816 | Missense Mutation | AGC,GGC | S,G 1860 | XP_016882559.1 | |
XM_017027071.1 | 5816 | Missense Mutation | AGC,GGC | S,G 1856 | XP_016882560.1 | |
XM_017027072.1 | 5816 | Missense Mutation | AGC,GGC | S,G 1847 | XP_016882561.1 | |
XM_017027073.1 | 5816 | Missense Mutation | AGC,GGC | S,G 1634 | XP_016882562.1 | |
XM_017027074.1 | 5816 | Missense Mutation | AGC,GGC | S,G 1458 | XP_016882563.1 | |
XM_017027075.1 | 5816 | Missense Mutation | AGC,GGC | S,G 1454 | XP_016882564.1 | |
XM_017027076.1 | 5816 | Missense Mutation | AGC,GGC | S,G 1442 | XP_016882565.1 |