Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GACTTTGGAGACTCAACCGTTAGCT[C/T]CGGACTGCTGTCCTTCAGACCAGGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 191170 MIM: 612661 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
TP53 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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TP53 - tumor protein p53 | ||||||
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There are no transcripts associated with this gene. |
WRAP53 - WD repeat containing antisense to TP53 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001143990.1 | 186 | Missense Mutation | CCG,TCG | P,S 11 | NP_001137462.1 | |
NM_001143991.1 | 186 | Missense Mutation | CCG,TCG | P,S 11 | NP_001137463.1 | |
NM_001143992.1 | 186 | Missense Mutation | CCG,TCG | P,S 11 | NP_001137464.1 | |
NM_018081.2 | 186 | Missense Mutation | CCG,TCG | P,S 11 | NP_060551.2 | |
XM_011523952.2 | 186 | Intron | XP_011522254.1 | |||
XM_017024812.1 | 186 | Missense Mutation | CCG,TCG | P,S 11 | XP_016880301.1 |