Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCTTCTCTCCCTGCGCCCAAGGGTC[A/C]GGCCTTGCTGCCTCCGCCCCCTCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
6 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 |
---|---|---|
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 |
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 | 433 | Missense Mutation | CAG,CCG | Q,P 48 | NP_005964.3 | |
XM_005245313.2 | 433 | Missense Mutation | CAG,CCG | Q,P 48 | XP_005245370.1 | |
XM_005245314.1 | 433 | Missense Mutation | CAG,CCG | Q,P 48 | XP_005245371.1 | |
XM_011509726.1 | 433 | Missense Mutation | CAG,CCG | Q,P 48 | XP_011508028.1 |