Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
61 submissions
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Phenotype: |
MIM: 164850 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
MYCL 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) - 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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MYCL - v-myc avian myelocytomatosis viral oncogene lung carcinoma derived homolog | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001033081.2 | 1666 | Missense Mutation | ACT,AGT | T,S 362 | NP_001028253.1 | |
NM_001033082.2 | 1666 | Missense Mutation | ACT,AGT | T,S 392 | NP_001028254.2 | |
NM_005376.4 | 1666 | Intron | NP_005367.2 |
Set Membership: |
HapMap |