Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGTGAAACCGTTCTCTTTACTGAAC[C/T]GGTCAATCTGGTCCCGGCTCACTGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
MIM: 603949 | ||||||||||||||||||||
Literature Links: |
RAB29 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 |
RAB29 - RAB29, member RAS oncogene family | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001135662.1 | 368 | Missense Mutation | CAG,CGG | Q,R 141 | NP_001129134.1 | |
NM_001135663.1 | 368 | Missense Mutation | CAG,CGG | Q,R 117 | NP_001129135.1 | |
NM_001135664.1 | 368 | Missense Mutation | CAG,CGG | Q,R 69 | NP_001129136.1 | |
NM_003929.2 | 368 | Missense Mutation | CAG,CGG | Q,R 141 | NP_003920.1 | |
XM_005245569.1 | 368 | Missense Mutation | CAG,CGG | Q,R 141 | XP_005245626.1 | |
XM_005245570.1 | 368 | Missense Mutation | CAG,CGG | Q,R 141 | XP_005245627.1 | |
XM_005245571.1 | 368 | Missense Mutation | CAG,CGG | Q,R 141 | XP_005245628.1 | |
XM_006711605.3 | 368 | Missense Mutation | CAG,CGG | Q,R 69 | XP_006711668.1 | |
XM_006711606.2 | 368 | Missense Mutation | CAG,CGG | Q,R 69 | XP_006711669.1 | |
XM_017002748.1 | 368 | Missense Mutation | CAG,CGG | Q,R 117 | XP_016858237.1 | |
XM_017002749.1 | 368 | Missense Mutation | CAG,CGG | Q,R 117 | XP_016858238.1 | |
XM_017002750.1 | 368 | Missense Mutation | CAG,CGG | Q,R 117 | XP_016858239.1 |