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CTGAGGCCCCTGAGGCTGCCGCTCA[A/C]TGGGGAAGGGCCTTGAGGATGGCGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601698 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PTPRN2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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PTPRN2 - protein tyrosine phosphatase, receptor type N2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | 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 |