Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGAGCTGGCTCCGTGCTTGACCTTC[A/C]CTCCCTTGGTGAAGGTCCGCTTCTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601619 | ||||||||||||||||||||
Literature Links: |
RALGDS 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 |
RALGDS - ral guanine nucleotide dissociation stimulator | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001042368.2 | 2746 | Missense Mutation | GGG,GTG | G,V 834 | NP_001035827.1 | |
NM_001271774.1 | 2746 | Missense Mutation | GGG,GTG | G,V 860 | NP_001258703.1 | |
NM_001271775.1 | 2746 | Missense Mutation | GGG,GTG | G,V 888 | NP_001258704.1 | |
NM_001271776.1 | 2746 | Missense Mutation | GGG,GTG | G,V 877 | NP_001258705.1 | |
NM_006266.3 | 2746 | Missense Mutation | GGG,GTG | G,V 889 | NP_006257.1 |