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GAGAACATGACTCCAATAAGGCTCA[C/T]GGCTGCCAAGCCCATTCCTGCAACG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613866 MIM: 613867 | ||||||||||||||||||||
Literature Links: |
HRASLS2 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 |
HRASLS2 - HRAS like suppressor 2 | ||||||
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There are no transcripts associated with this gene. |
PLA2G16 - phospholipase A2 group XVI | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001128203.1 | 764 | Missense Mutation | ATG,GTG | M,V 147 | NP_001121675.1 | |
NM_007069.3 | 764 | Missense Mutation | ATG,GTG | M,V 147 | NP_009000.2 | |
XM_006718426.1 | 764 | Missense Mutation | ATG,GTG | M,V 147 | XP_006718489.1 | |
XM_011544741.1 | 764 | Missense Mutation | ATG,GTG | M,V 162 | XP_011543043.1 |