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AAAGATGGCCGGGAACTCGATCCTG[C/T]TGGCTGCTGTCTCTATTCTCTCGGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601733 | ||||||||||||||||||||
Literature Links: |
MGST2 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 |
MGST2 - microsomal glutathione S-transferase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001204366.1 | 61 | Silent Mutation | CTG,TTG | L,L 8 | NP_001191295.1 | |
NM_001204367.1 | 61 | UTR 5 | NP_001191296.1 | |||
NM_001204368.1 | 61 | Silent Mutation | CTG,TTG | L,L 8 | NP_001191297.1 | |
NM_002413.4 | 61 | Silent Mutation | CTG,TTG | L,L 8 | NP_002404.1 | |
XM_006714221.2 | 61 | UTR 5 | XP_006714284.1 | |||
XM_011531972.2 | 61 | Intron | XP_011530274.1 | |||
XM_017008211.1 | 61 | Silent Mutation | CTG,TTG | L,L 8 | XP_016863700.1 | |
XM_017008212.1 | 61 | Silent Mutation | CTG,TTG | L,L 8 | XP_016863701.1 | |
XM_017008213.1 | 61 | Silent Mutation | CTG,TTG | L,L 8 | XP_016863702.1 | |
XM_017008214.1 | 61 | UTR 5 | XP_016863703.1 |