Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGCGTCCGCCTGCGGTGCCACTGG[C/T]GCAGGGAGGCGCGGGCCTCGGAGCT
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 |
---|---|---|
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 |
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 | 1571 | Missense Mutation | CAC,CGC | H,R 529 | NP_001182762.1 | |
NM_198445.3 | 1571 | Intron | NP_940847.1 | |||
XM_006723015.2 | 1571 | Missense Mutation | CAC,CGC | H,R 529 | XP_006723078.1 | |
XM_006723016.2 | 1571 | Missense Mutation | CAC,CGC | H,R 415 | XP_006723079.1 | |
XM_011526454.2 | 1571 | Missense Mutation | CAC,CGC | H,R 529 | XP_011524756.1 | |
XM_011526455.2 | 1571 | Missense Mutation | CAC,CGC | H,R 497 | XP_011524757.1 |
SIRT2 - sirtuin 2 | ||||||
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There are no transcripts associated with this gene. |