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GCCAGATGTTCAGCAGCAGCCAGAG[G/T]TGGACCCTATGTCACGAGAGTTCCG
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607466 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
RAB2B 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)
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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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RAB2B - RAB2B, member RAS oncogene family | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001163380.1 | 663 | Missense Mutation | AAC,ACC | N,T 166 | NP_001156852.1 | |
NM_032846.3 | 663 | Missense Mutation | AAC,ACC | N,T 212 | NP_116235.2 | |
XM_017021710.1 | 663 | Missense Mutation | AAC,ACC | N,T 167 | XP_016877199.1 | |
XM_017021711.1 | 663 | Missense Mutation | AAC,ACC | N,T 147 | XP_016877200.1 | |
XM_017021712.1 | 663 | Missense Mutation | AAC,ACC | N,T 143 | XP_016877201.1 |