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Search Thermo Fisher Scientific
CCCCTGGAAAACCTCCCATGGCTCC[C/G]CCTTCTAAAGAACCTCCTGGCAGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
6 submissions
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Phenotype: |
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Literature Links: |
ATXN7L2 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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ATXN7L2 - ataxin 7 like 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_153340.4 | 576 | Silent Mutation | CCC,CCG | P,P 187 | NP_699171.3 | |
XM_005270445.3 | 576 | Silent Mutation | CCC,CCG | P,P 219 | XP_005270502.1 | |
XM_005270446.2 | 576 | Silent Mutation | CCC,CCG | P,P 219 | XP_005270503.1 | |
XM_011540638.2 | 576 | Silent Mutation | CCC,CCG | P,P 197 | XP_011538940.1 | |
XM_011540639.2 | 576 | Silent Mutation | CCC,CCG | P,P 161 | XP_011538941.1 | |
XM_011540641.2 | 576 | Silent Mutation | CCC,CCG | P,P 161 | XP_011538943.1 | |
XM_011540644.2 | 576 | Silent Mutation | CCC,CCG | P,P 161 | XP_011538946.1 | |
XM_011540645.1 | 576 | Missense Mutation | CCC,CGC | P,R 32 | XP_011538947.1 | |
XM_011540646.2 | 576 | Silent Mutation | CCC,CCG | P,P 219 | XP_011538948.1 | |
XM_017000267.1 | 576 | Silent Mutation | CCC,CCG | P,P 161 | XP_016855756.1 | |
XM_017000268.1 | 576 | Silent Mutation | CCC,CCG | P,P 161 | XP_016855757.1 | |
XM_017000269.1 | 576 | Silent Mutation | CCC,CCG | P,P 161 | XP_016855758.1 | |
XM_017000270.1 | 576 | Silent Mutation | CCC,CCG | P,P 161 | XP_016855759.1 |
CYB561D1 - cytochrome b561 family member D1 | ||||||
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There are no transcripts associated with this gene. |
SYPL2 - synaptophysin like 2 | ||||||
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There are no transcripts associated with this gene. |