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CTCCGGAACAAACGTGAGGTCTGGA[G/T]GGTCAAATTTACCCTGGCCAAGATC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603631 MIM: 608754 | ||||||||||||||||||||
Literature Links: |
RPS9 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 |
RPS9 - ribosomal protein S9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001013.3 | 496 | Intron | NP_001004.2 | |||
NM_001321701.1 | 496 | Intron | NP_001308630.1 | |||
NM_001321702.1 | 496 | Intron | NP_001308631.1 | |||
NM_001321704.1 | 496 | Intron | NP_001308633.1 | |||
NM_001321705.1 | 496 | Intron | NP_001308634.1 | |||
NM_001321706.1 | 496 | Intron | NP_001308635.1 | |||
XM_017027112.1 | 496 | Missense Mutation | AGG,ATG | R,M 45 | XP_016882601.1 |
TSEN34 - tRNA splicing endonuclease subunit 34 | ||||||
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There are no transcripts associated with this gene. |