Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGCCAGAGTTGGACCCTATGTCAC[A/G]AGAGTTCCGCTGGGAGGCACTGGGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 607466 | ||||||||||||||||||||
Literature Links: |
RAB2B PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
RAB2B - RAB2B, member RAS oncogene family | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001163380.1 | 647 | Missense Mutation | AGT,GGT | S,G 161 | NP_001156852.1 | |
NM_032846.3 | 647 | Missense Mutation | AGT,GGT | S,G 207 | NP_116235.2 | |
XM_017021710.1 | 647 | Missense Mutation | AGT,GGT | S,G 162 | XP_016877199.1 | |
XM_017021711.1 | 647 | Missense Mutation | AGT,GGT | S,G 142 | XP_016877200.1 | |
XM_017021712.1 | 647 | Missense Mutation | AGT,GGT | S,G 138 | XP_016877201.1 |