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CCCTCCCTTACCTTGGTTCTCGCCT[C/T]GAGCCAGGCCCGCATAGACATCTCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604480 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RINL 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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RINL - Ras and Rab interactor like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001195833.1 | 1313 | Missense Mutation | CAA,CGA | Q,R 443 | NP_001182762.1 | |
NM_198445.3 | 1313 | Intron | NP_940847.1 | |||
XM_006723015.2 | 1313 | Missense Mutation | CAA,CGA | Q,R 443 | XP_006723078.1 | |
XM_006723016.2 | 1313 | Missense Mutation | CAA,CGA | Q,R 329 | XP_006723079.1 | |
XM_011526454.2 | 1313 | Missense Mutation | CAA,CGA | Q,R 443 | XP_011524756.1 | |
XM_011526455.2 | 1313 | Missense Mutation | CAA,CGA | Q,R 411 | XP_011524757.1 |
SIRT2 - sirtuin 2 | ||||||
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There are no transcripts associated with this gene. |