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GAGCTGGCTCCGTGCTTGACCTTCA[C/T]TCCCTTGGTGAAGGTCCGCTTCTTG
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 | |||
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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) - Not Available | |||
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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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 | 2745 | Missense Mutation | ATG,GTG | M,V 834 | NP_001035827.1 | |
NM_001271774.1 | 2745 | Missense Mutation | ATG,GTG | M,V 860 | NP_001258703.1 | |
NM_001271775.1 | 2745 | Missense Mutation | ATG,GTG | M,V 888 | NP_001258704.1 | |
NM_001271776.1 | 2745 | Missense Mutation | ATG,GTG | M,V 877 | NP_001258705.1 | |
NM_006266.3 | 2745 | Missense Mutation | ATG,GTG | M,V 889 | NP_006257.1 |