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ATCTTACATTGTCAAATATAAGGAA[A/G]TTTGTCCGTGGATGCAAACAGTATA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603317 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PTPRQ 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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PTPRQ - protein tyrosine phosphatase, receptor type Q | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145026.1 | 1088 | Missense Mutation | ATT,GTT | I,V 96 | NP_001138498.1 | |
XM_017019273.1 | 1088 | Missense Mutation | ATT,GTT | I,V 318 | XP_016874762.1 | |
XM_017019274.1 | 1088 | Missense Mutation | ATT,GTT | I,V 318 | XP_016874763.1 | |
XM_017019275.1 | 1088 | Missense Mutation | ATT,GTT | I,V 318 | XP_016874764.1 |