Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GATCTCGGCTCACTGCAACCTCAAC[A/G]GTGCTTTTTTCTGATCATAGCTGAG
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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
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 | 5071 | Missense Mutation | CCG,CTG | P,L 116 | NP_001182123.1 | |
NM_001195195.1 | 5071 | Intron | NP_001182124.1 | |||
NM_001251964.1 | 5071 | UTR 3 | NP_001238893.1 | |||
NM_022112.2 | 5071 | Missense Mutation | CCG,CTG | P,L 120 | NP_071395.2 | |
XM_017018113.1 | 5071 | Missense Mutation | CCG,CTG | P,L 142 | XP_016873602.1 | |
XM_017018114.1 | 5071 | Missense Mutation | CCG,CTG | P,L 138 | XP_016873603.1 | |
XM_017018115.1 | 5071 | Intron | XP_016873604.1 | |||
XM_017018116.1 | 5071 | Missense Mutation | CCG,CTG | P,L 120 | XP_016873605.1 | |
XM_017018117.1 | 5071 | Intron | XP_016873606.1 |