Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGCCACCTCGCCACGAACTCAGCCC[A/G]CCACAGAAGCGCATGAGGAGAGACT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 100740 MIM: 614469 MIM: 602933 MIM: 611481 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ACHE 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
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CEPH (CEU) - Not Available | ||||||
EAS
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African American
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YRI (Yoruba) - Not Available | ||||||
SAS
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Japanese
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CHB (Han Chinese) - Not Available | ||||||
AFR
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Chinese
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JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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ACHE - acetylcholinesterase (Cartwright blood group) | ||||||
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There are no transcripts associated with this gene. |
SRRT - serrate, RNA effector molecule | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001128852.1 | 493 | Silent Mutation | CCA,CCG | P,P 75 | NP_001122324.1 | |
NM_001128853.1 | 493 | Silent Mutation | CCA,CCG | P,P 75 | NP_001122325.1 | |
NM_001128854.1 | 493 | Silent Mutation | CCA,CCG | P,P 75 | NP_001122326.1 | |
NM_015908.5 | 493 | Silent Mutation | CCA,CCG | P,P 75 | NP_056992.4 | |
XM_005250405.2 | 493 | Silent Mutation | CCA,CCG | P,P 82 | XP_005250462.1 | |
XM_005250406.2 | 493 | Silent Mutation | CCA,CCG | P,P 82 | XP_005250463.1 | |
XM_005250407.2 | 493 | Silent Mutation | CCA,CCG | P,P 82 | XP_005250464.1 | |
XM_005250408.2 | 493 | Silent Mutation | CCA,CCG | P,P 82 | XP_005250465.1 | |
XM_017012290.1 | 493 | UTR 5 | XP_016867779.1 | |||
XM_017012291.1 | 493 | UTR 5 | XP_016867780.1 |
TRIP6 - thyroid hormone receptor interactor 6 | ||||||
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There are no transcripts associated with this gene. |
UFSP1 - UFM1 specific peptidase 1 (inactive) | ||||||
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There are no transcripts associated with this gene. |