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CGTTGTGGTCGGCGGTGCAGTAGGC[A/G]ATGCGGGCCACCTGGAAGGTATCCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612930 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PID1 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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PID1 - phosphotyrosine interaction domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001100818.1 | 697 | Silent Mutation | ATC,ATT | I,I 133 | NP_001094288.1 | |
NM_017933.4 | 697 | Silent Mutation | ATC,ATT | I,I 164 | NP_060403.3 | |
XM_011511384.2 | 697 | Silent Mutation | ATC,ATT | I,I 166 | XP_011509686.1 | |
XM_017004404.1 | 697 | Silent Mutation | ATC,ATT | I,I 221 | XP_016859893.1 | |
XM_017004405.1 | 697 | Silent Mutation | ATC,ATT | I,I 184 | XP_016859894.1 | |
XM_017004406.1 | 697 | Silent Mutation | ATC,ATT | I,I 119 | XP_016859895.1 | |
XM_017004407.1 | 697 | Silent Mutation | ATC,ATT | I,I 84 | XP_016859896.1 |