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TCAGATGCTGGCGCCAGCCTTTCCC[A/C]CGCCGCTGTTGCTTCCCCCACCCAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
3 submissions
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Phenotype: |
MIM: 179755 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PRCC 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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PRCC - papillary renal cell carcinoma (translocation-associated) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005973.4 | 480 | Missense Mutation | ACG,CCG | T,P 64 | NP_005964.3 | |
XM_005245313.2 | 480 | Missense Mutation | ACG,CCG | T,P 64 | XP_005245370.1 | |
XM_005245314.1 | 480 | Missense Mutation | ACG,CCG | T,P 64 | XP_005245371.1 | |
XM_011509726.1 | 480 | Missense Mutation | ACG,CCG | T,P 64 | XP_011508028.1 |