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Search Thermo Fisher Scientific
TTTGGGGCCCCCTGTGAGCCGCGAC[C/T]GTGTCATCGCCAGCTTCCCTAAGGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 605662 MIM: 605663 | ||||||||||||||||||||
Literature Links: |
RAB36 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 |
RAB36 - RAB36, member RAS oncogene family | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004914.3 | 296 | Missense Mutation | CGT,TGT | R,C 82 | NP_004905.2 | |
XM_005261859.4 | 296 | Missense Mutation | CGT,TGT | R,C 106 | XP_005261916.1 | |
XM_006724381.3 | 296 | Missense Mutation | CGT,TGT | R,C 106 | XP_006724444.1 | |
XM_006724382.3 | 296 | Missense Mutation | CGT,TGT | R,C 82 | XP_006724445.1 | |
XM_011530544.2 | 296 | Missense Mutation | CGT,TGT | R,C 106 | XP_011528846.1 | |
XM_011530545.2 | 296 | Missense Mutation | CGT,TGT | R,C 106 | XP_011528847.1 | |
XM_011530546.2 | 296 | Missense Mutation | CGT,TGT | R,C 106 | XP_011528848.1 | |
XM_011530547.2 | 296 | Intron | XP_011528849.1 | |||
XM_011530550.2 | 296 | Missense Mutation | CGT,TGT | R,C 106 | XP_011528852.1 | |
XM_011530552.2 | 296 | Intron | XP_011528854.1 | |||
XM_017029104.1 | 296 | Intron | XP_016884593.1 | |||
XM_017029105.1 | 296 | Intron | XP_016884594.1 | |||
XM_017029106.1 | 296 | Intron | XP_016884595.1 | |||
XM_017029107.1 | 296 | Intron | XP_016884596.1 |
RSPH14 - radial spoke head 14 homolog | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014433.2 | 296 | Intron | NP_055248.1 | |||
XM_011530149.2 | 296 | Intron | XP_011528451.1 | |||
XM_011530150.1 | 296 | Intron | XP_011528452.1 | |||
XM_011530151.2 | 296 | Intron | XP_011528453.1 | |||
XM_011530152.2 | 296 | Intron | XP_011528454.1 | |||
XM_011530154.2 | 296 | Intron | XP_011528456.1 | |||
XM_011530155.2 | 296 | Intron | XP_011528457.1 | |||
XM_017028774.1 | 296 | Intron | XP_016884263.1 |