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GTGCCCACGCCGGGCGCTGCACAAG[C/G]AGAAAGACGGCACTGAGTTCAAGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603000 | ||||||||||||||||||||
Literature Links: |
CDR2L 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 |
CDR2L - cerebellar degeneration related protein 2 like | ||||||
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There are no transcripts associated with this gene. |
MRPL58 - mitochondrial ribosomal protein L58 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001303265.1 | 120 | Missense Mutation | CAG,GAG | Q,E 33 | NP_001290194.1 | |
NM_001545.2 | 120 | Missense Mutation | CAG,GAG | Q,E 33 | NP_001536.1 | |
XM_017024574.1 | 120 | Intron | XP_016880063.1 |