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TGGTGAGTCTGAAAACTTGGGATGT[C/T]GGCACCACGGTGAGAGCAGAGTCTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605426 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TP53AIP1 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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TP53AIP1 - tumor protein p53 regulated apoptosis inducing protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001195194.1 | 902 | Intron | NP_001182123.1 | |||
NM_001195195.1 | 902 | Intron | NP_001182124.1 | |||
NM_001251964.1 | 902 | Missense Mutation | AAC,GAC | N,D 74 | NP_001238893.1 | |
NM_022112.2 | 902 | Intron | NP_071395.2 | |||
XM_017018113.1 | 902 | Intron | XP_016873602.1 | |||
XM_017018114.1 | 902 | Intron | XP_016873603.1 | |||
XM_017018115.1 | 902 | Intron | XP_016873604.1 | |||
XM_017018116.1 | 902 | Intron | XP_016873605.1 | |||
XM_017018117.1 | 902 | Intron | XP_016873606.1 |