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TGAAATAACTGCTCCAGCAGCCTTC[A/G]CTCCTTCCATCAGGGCGTGCTCTAC
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611474 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
HRASLS5 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)
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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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HRASLS5 - HRAS like suppressor family member 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001146728.1 | 771 | Silent Mutation | NP_001140200.1 | |||
NM_001146729.1 | 771 | Missense Mutation | NP_001140201.1 | |||
NM_054108.3 | 771 | Missense Mutation | NP_473449.1 | |||
XM_011544751.2 | 771 | Missense Mutation | XP_011543053.1 | |||
XM_011544752.2 | 771 | Missense Mutation | XP_011543054.1 | |||
XM_011544753.1 | 771 | Missense Mutation | XP_011543055.1 | |||
XM_017017172.1 | 771 | Missense Mutation | XP_016872661.1 |