Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGTTCCTGTCACCGCCTCTTCCCT[C/T]CGTGAGCGCTGGCCTGGGGGAACCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606492 | ||||||||||||||||||||
Literature Links: |
EXOSC5 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 |
EXOSC5 - exosome component 5 | ||||||
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There are no transcripts associated with this gene. |
TMEM91 - transmembrane protein 91 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001042595.2 | 326 | Missense Mutation | TCC,TTC | S,F 56 | NP_001036060.1 | |
NM_001098821.1 | 326 | Missense Mutation | TCC,TTC | S,F 56 | NP_001092291.1 | |
NM_001098822.1 | 326 | Missense Mutation | TCC,TTC | S,F 56 | NP_001092292.1 | |
NM_001098823.1 | 326 | Missense Mutation | TCC,TTC | S,F 56 | NP_001092293.1 | |
NM_001098824.1 | 326 | Missense Mutation | TCC,TTC | S,F 56 | NP_001092294.1 | |
NM_001098825.1 | 326 | Missense Mutation | TCC,TTC | S,F 56 | NP_001092295.1 |