Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ALS2CR11 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
ALS2CR11 - amyotrophic lateral sclerosis 2 chromosome region candidate 11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001168216.1 | 4713 | Intron | NP_001161688.1 | |||
NM_001168217.1 | 4713 | Intron | NP_001161689.1 | |||
NM_001168221.1 | 4713 | Missense Mutation | AAT,ATT | N,I 1554 | NP_001161693.1 | |
NM_152525.5 | 4713 | Intron | NP_689738.3 | |||
XM_006712331.3 | 4713 | Intron | XP_006712394.1 | |||
XM_006712332.3 | 4713 | Intron | XP_006712395.1 | |||
XM_006712333.3 | 4713 | Intron | XP_006712396.1 | |||
XM_006712334.3 | 4713 | Intron | XP_006712397.1 | |||
XM_006712335.3 | 4713 | Intron | XP_006712398.1 | |||
XM_006712336.3 | 4713 | Intron | XP_006712399.1 | |||
XM_011510736.2 | 4713 | Intron | XP_011509038.1 |