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CGTCCTTCATGAGCTCCTCGATGTC[A/G]TCCTCCGTGATGGTCTCGCCTGTAG
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615507 MIM: 191040 | |||||||||||||||||||||||
Literature Links: |
NISCH 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 - 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 |
NISCH - nischarin | ||||||
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There are no transcripts associated with this gene. |
SEMA3G - semaphorin 3G | ||||||
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There are no transcripts associated with this gene. |
TNNC1 - troponin C1, slow skeletal and cardiac type | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003280.2 | 419 | Silent Mutation | GAC,GAT | D,D 131 | NP_003271.1 |