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TGATGGAGGAGATGGGTGTCACCTC[C/T]ATAGGCAGTGCCAAGGAAGACAGCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612177 MIM: 603633 | ||||||||||||||||||||
Literature Links: |
RN7SL1 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 |
RN7SL1 - RNA, 7SL, cytoplasmic 1 | ||||||
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There are no transcripts associated with this gene. |
RPS29 - ribosomal protein S29 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001030001.2 | 267 | Nonsense Mutation | NP_001025172.1 | |||
NM_001032.4 | 267 | Intron | NP_001023.1 |