Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGAGCAGCTCTCGTAGCCATTTCAA[A/G]AACCTCTCTCACTCCATCTTTGGTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 138320 MIM: 165390 | ||||||||||||||||||||
Literature Links: |
GPX1 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 |
GPX1 - glutathione peroxidase 1 | ||||||
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There are no transcripts associated with this gene. |
RHOA - ras homolog family member A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001313941.1 | 668 | Missense Mutation | CTT,TTT | L,F 171 | NP_001300870.1 | |
NM_001313943.1 | 668 | UTR 3 | NP_001300872.1 | |||
NM_001313944.1 | 668 | Missense Mutation | CTT,TTT | L,F 151 | NP_001300873.1 | |
NM_001313945.1 | 668 | Missense Mutation | CTT,TTT | L,F 90 | NP_001300874.1 | |
NM_001313946.1 | 668 | Missense Mutation | CTT,TTT | L,F 87 | NP_001300875.1 | |
NM_001313947.1 | 668 | UTR 3 | NP_001300876.1 | |||
NM_001664.3 | 668 | Missense Mutation | CTT,TTT | L,F 171 | NP_001655.1 |