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AATAGCTTTTCGGAAACAGTGGAAG[G/T]TGTAGTCTATTAAACCTGCAGGAAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
2 submissions
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Phenotype: |
MIM: 608267 | ||||||||||||||||||||
Literature Links: |
RRAGC 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 |
RRAGC - Ras related GTP binding C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271851.1 | 1139 | Missense Mutation | AAC,ACC | N,T 321 | NP_001258780.1 | |
NM_022157.3 | 1139 | Missense Mutation | AAC,ACC | N,T 355 | NP_071440.1 |