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TTTCCATGTGTTGGGTTAAGGCAGA[A/G]CGAAATACTTCTACTGCAAAATCAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612471 | ||||||||||||||||||||
Literature Links: |
AGXT2 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 |
AGXT2 - alanine--glyoxylate aminotransferase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001306173.1 | 1799 | Silent Mutation | CGC,CGT | R,R 427 | NP_001293102.1 | |
NM_031900.3 | 1799 | Silent Mutation | CGC,CGT | R,R 502 | NP_114106.1 | |
XM_005248337.2 | 1799 | Silent Mutation | CGC,CGT | R,R 501 | XP_005248394.1 | |
XM_005248338.2 | 1799 | Silent Mutation | CGC,CGT | R,R 437 | XP_005248395.1 | |
XM_017009748.1 | 1799 | Silent Mutation | CGC,CGT | R,R 427 | XP_016865237.1 |