Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
37 submissions
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Phenotype: |
MIM: 126110 MIM: 601105 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ARNT 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 | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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ARNT - aryl hydrocarbon receptor nuclear translocator | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001197325.1 | 2148 | Missense Mutation | CCT,CTT | P,L 690 | NP_001184254.1 | |
NM_001286035.1 | 2148 | Missense Mutation | CCT,CTT | P,L 692 | NP_001272964.1 | |
NM_001286036.1 | 2148 | Missense Mutation | CCT,CTT | P,L 704 | NP_001272965.1 | |
NM_001668.3 | 2148 | Missense Mutation | CCT,CTT | P,L 706 | NP_001659.1 | |
NM_178427.2 | 2148 | Missense Mutation | CCT,CTT | P,L 691 | NP_848514.1 | |
XM_005245151.1 | 2148 | Missense Mutation | CCT,CTT | P,L 705 | XP_005245208.1 | |
XM_005245153.1 | 2148 | Missense Mutation | CCT,CTT | P,L 701 | XP_005245210.1 | |
XM_005245154.3 | 2148 | Missense Mutation | CCT,CTT | P,L 697 | XP_005245211.1 | |
XM_005245157.1 | 2148 | Missense Mutation | CCT,CTT | P,L 669 | XP_005245214.1 | |
XM_011509542.2 | 2148 | Missense Mutation | CCT,CTT | P,L 705 | XP_011507844.1 | |
XM_011509543.2 | 2148 | Missense Mutation | CCT,CTT | P,L 705 | XP_011507845.1 | |
XM_011509544.2 | 2148 | Missense Mutation | CCT,CTT | P,L 704 | XP_011507846.1 | |
XM_011509545.2 | 2148 | Missense Mutation | CCT,CTT | P,L 690 | XP_011507847.1 | |
XM_011509546.1 | 2148 | Missense Mutation | CCT,CTT | P,L 674 | XP_011507848.1 | |
XM_011509547.2 | 2148 | Missense Mutation | CCT,CTT | P,L 689 | XP_011507849.1 | |
XM_017001288.1 | 2148 | Missense Mutation | CCT,CTT | P,L 696 | XP_016856777.1 | |
XM_017001289.1 | 2148 | Missense Mutation | CCT,CTT | P,L 692 | XP_016856778.1 | |
XM_017001290.1 | 2148 | Missense Mutation | CCT,CTT | P,L 682 | XP_016856779.1 | |
XM_017001291.1 | 2148 | Missense Mutation | CCT,CTT | P,L 681 | XP_016856780.1 | |
XM_017001292.1 | 2148 | Missense Mutation | CCT,CTT | P,L 660 | XP_016856781.1 | |
XM_017001293.1 | 2148 | Missense Mutation | CCT,CTT | P,L 644 | XP_016856782.1 | |
XM_017001294.1 | 2148 | Missense Mutation | CCT,CTT | P,L 668 | XP_016856783.1 | |
XM_017001295.1 | 2148 | Missense Mutation | CCT,CTT | P,L 664 | XP_016856784.1 | |
XM_017001296.1 | 2148 | Missense Mutation | CCT,CTT | P,L 654 | XP_016856785.1 |
CTSK - cathepsin K | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap JSNP |