Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGCAGGGGCATACCCATCCAGGGAG[G/T]AGGGAAGGGGAAACCAGGGGCAGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 134690 MIM: 606866 MIM: 608046 | ||||||||||||||||||||
Literature Links: |
FAU PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
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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 |
FAU - FAU, ubiquitin like and ribosomal protein S30 fusion | ||||||
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There are no transcripts associated with this gene. |
MIR6751 - microRNA 6751 | ||||||
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There are no transcripts associated with this gene. |
MRPL49 - mitochondrial ribosomal protein L49 | ||||||
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There are no transcripts associated with this gene. |
SYVN1 - synoviolin 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032431.2 | 2314 | Missense Mutation | ACT,CCT | T,P 457 | NP_115807.1 | |
NM_172230.2 | 2314 | Missense Mutation | ACT,CCT | T,P 458 | NP_757385.1 | |
XM_011545303.2 | 2314 | Missense Mutation | ACT,CCT | T,P 458 | XP_011543605.1 |