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AAATGCGAATCCTAAAGCGTTTCCT[C/T]GCTTGCATTCAGCTCCTCTGTGTTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 176891 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PTPRZ1 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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PTPRZ1 - protein tyrosine phosphatase, receptor type Z1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001206838.1 | 419 | Silent Mutation | CTC,CTT | L,L 8 | NP_001193767.1 | |
NM_001206839.1 | 419 | Silent Mutation | CTC,CTT | L,L 8 | NP_001193768.1 | |
NM_002851.2 | 419 | Silent Mutation | CTC,CTT | L,L 8 | NP_002842.2 | |
XM_005250519.1 | 419 | Silent Mutation | CTC,CTT | L,L 8 | XP_005250576.1 | |
XM_017012477.1 | 419 | UTR 5 | XP_016867966.1 |