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ATTCCAACAGCCCAGCTGTGCCCTG[C/T]CGGTGCTGCCAGGAGCACGGTCCGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
13 submissions
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Phenotype: |
MIM: 134629 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FDPS 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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FDPS - farnesyl diphosphate synthase | ||||||
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There are no transcripts associated with this gene. |
LOC105371451 - uncharacterized LOC105371451 | ||||||
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There are no transcripts associated with this gene. |
RUSC1 - RUN and SH3 domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001105203.1 | 442 | Silent Mutation | TGC,TGT | C,C 71 | NP_001098673.1 | |
NM_001105204.1 | 442 | Silent Mutation | TGC,TGT | C,C 71 | NP_001098674.1 | |
NM_001105205.1 | 442 | Intron | NP_001098675.1 | |||
NM_001278227.1 | 442 | Intron | NP_001265156.1 | |||
NM_001278228.1 | 442 | Intron | NP_001265157.1 | |||
NM_001278229.1 | 442 | Intron | NP_001265158.1 | |||
NM_001278230.1 | 442 | Intron | NP_001265159.1 | |||
NM_014328.4 | 442 | Intron | NP_055143.2 | |||
XM_006711254.1 | 442 | Silent Mutation | TGC,TGT | C,C 71 | XP_006711317.1 | |
XM_006711256.1 | 442 | Silent Mutation | TGC,TGT | C,C 71 | XP_006711319.1 | |
XM_006711257.1 | 442 | Intron | XP_006711320.1 | |||
XM_017000891.1 | 442 | Silent Mutation | TGC,TGT | C,C 71 | XP_016856380.1 | |
XM_017000892.1 | 442 | Intron | XP_016856381.1 |
RUSC1-AS1 - RUSC1 antisense RNA 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001039517.1 | 442 | Intron | NP_001034606.1 |