Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCAGGGGACTTGATCGAAGTGTTCC[A/G]TCCTGGCTATCAGCACTGGGCCCTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606487 | ||||||||||||||||||||
Literature Links: |
HRASLS 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 |
HRASLS - HRAS like suppressor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020386.4 | 480 | Missense Mutation | CAT,CGT | H,R 130 | NP_065119.2 | |
XM_011513034.1 | 480 | Missense Mutation | CAT,CGT | H,R 130 | XP_011511336.1 | |
XM_011513035.2 | 480 | Missense Mutation | CAT,CGT | H,R 130 | XP_011511337.1 | |
XM_011513037.2 | 480 | Intron | XP_011511339.1 | |||
XM_017006923.1 | 480 | Missense Mutation | CAT,CGT | H,R 25 | XP_016862412.1 |