Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 100740 MIM: 614469 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 - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | CHB (Han Chinese)
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AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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ACHE - acetylcholinesterase (Cartwright blood group) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000665.4 | 1357 | Silent Mutation | CCC,CCT | P,P 477 | NP_000656.1 | |
NM_001282449.1 | 1357 | Silent Mutation | CCC,CCT | P,P 389 | NP_001269378.1 | |
NM_001302621.1 | 1357 | Silent Mutation | CCC,CCT | P,P 477 | NP_001289550.1 | |
NM_001302622.1 | 1357 | Silent Mutation | CCC,CCT | P,P 477 | NP_001289551.1 | |
NM_015831.2 | 1357 | Silent Mutation | CCC,CCT | P,P 477 | NP_056646.1 | |
XM_006715995.2 | 1357 | Silent Mutation | CCC,CCT | P,P 477 | XP_006716058.1 | |
XM_011516225.1 | 1357 | Silent Mutation | CCC,CCT | P,P 643 | XP_011514527.1 | |
XM_011516226.1 | 1357 | Silent Mutation | CCC,CCT | P,P 555 | XP_011514528.1 | |
XM_011516228.2 | 1357 | Silent Mutation | CCC,CCT | P,P 477 | XP_011514530.1 | |
XM_011516229.2 | 1357 | Silent Mutation | CCC,CCT | P,P 477 | XP_011514531.1 | |
XM_017012219.1 | 1357 | Silent Mutation | CCC,CCT | P,P 643 | XP_016867708.1 | |
XM_017012220.1 | 1357 | Silent Mutation | CCC,CCT | P,P 555 | XP_016867709.1 |
SRRT - serrate, RNA effector molecule | ||||||
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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. |
Set Membership: |
HapMap |