Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTCAGGGAAGGGCTGACTACTAATG[C/G]CACGGAAGAGCTCCAGTGGATCCCG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604452 | ||||||||||||||||||||
Literature Links: |
PSMD5 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 |
PSMD5 - proteasome 26S subunit, non-ATPase 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001270427.1 | 1224 | Missense Mutation | GCC,GGC | A,G 358 | NP_001257356.1 | |
NM_005047.3 | 1224 | Missense Mutation | GCC,GGC | A,G 401 | NP_005038.1 | |
XM_011518866.2 | 1224 | Missense Mutation | GCC,GGC | A,G 401 | XP_011517168.1 | |
XM_017014927.1 | 1224 | Missense Mutation | GCC,GGC | A,G 401 | XP_016870416.1 | |
XM_017014928.1 | 1224 | Missense Mutation | GCC,GGC | A,G 187 | XP_016870417.1 |