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GCCTCCATGTATGTTACCTTAAGCT[A/G]CCGTGCTAACTGTTGTCCTTCTTCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600098 | ||||||||||||||||||||
Literature Links: |
RRAS2 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 |
RRAS2 - related RAS viral (r-ras) oncogene homolog 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001102669.2 | 605 | Nonsense Mutation | CAG,TAG | Q,* 71 | NP_001096139.1 | |
NM_001177314.1 | 605 | Intron | NP_001170785.1 | |||
NM_001177315.1 | 605 | Intron | NP_001170786.1 | |||
NM_012250.5 | 605 | Nonsense Mutation | CAG,TAG | Q,* 148 | NP_036382.2 | |
XM_017017363.1 | 605 | Intron | XP_016872852.1 |