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CTGTACACATCCACGGGTTCTGACA[A/G]ATCTGGGCCACTTAGGTCAAGGGCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600806 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CNN1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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CNN1 - calponin 1 | ||||||
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There are no transcripts associated with this gene. |
ELOF1 - elongation factor 1 homolog | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032377.3 | 408 | Silent Mutation | CTG,TTG | L,L 64 | NP_115753.1 | |
XM_017027356.1 | 408 | Silent Mutation | CTG,TTG | L,L 85 | XP_016882845.1 | |
XM_017027357.1 | 408 | Silent Mutation | CTG,TTG | L,L 71 | XP_016882846.1 | |
XM_017027358.1 | 408 | Silent Mutation | CTG,TTG | L,L 64 | XP_016882847.1 | |
XM_017027359.1 | 408 | Silent Mutation | CTG,TTG | L,L 64 | XP_016882848.1 |
LOC105369211 - uncharacterized LOC105369211 | ||||||
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There are no transcripts associated with this gene. |