Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGGATGGGTATGCCGCCATGGCAGC[A/C]CAGCCTCTCTTTGTGGCAGGATATC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
AGBL2 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 |
AGBL2 - ATP/GTP binding protein like 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024783.3 | 2463 | Missense Mutation | TGG,TGT | W,C 887 | NP_079059.2 | |
XM_005253138.4 | 2463 | Missense Mutation | TGG,TGT | W,C 849 | XP_005253195.1 | |
XM_005253139.4 | 2463 | Missense Mutation | TGG,TGT | W,C 813 | XP_005253196.1 | |
XM_005253140.4 | 2463 | Missense Mutation | TGG,TGT | W,C 771 | XP_005253197.1 | |
XM_005253141.4 | 2463 | Intron | XP_005253198.1 | |||
XM_006718327.3 | 2463 | Missense Mutation | TGG,TGT | W,C 831 | XP_006718390.1 | |
XM_006718328.3 | 2463 | Missense Mutation | TGG,TGT | W,C 795 | XP_006718391.1 | |
XM_011520372.2 | 2463 | Missense Mutation | TGG,TGT | W,C 849 | XP_011518674.1 | |
XM_011520373.2 | 2463 | Intron | XP_011518675.1 | |||
XM_011520374.2 | 2463 | Missense Mutation | TGG,TGT | W,C 813 | XP_011518676.1 | |
XM_011520375.2 | 2463 | Missense Mutation | TGG,TGT | W,C 804 | XP_011518677.1 | |
XM_011520376.2 | 2463 | Missense Mutation | TGG,TGT | W,C 751 | XP_011518678.1 | |
XM_011520377.2 | 2463 | Missense Mutation | TGG,TGT | W,C 751 | XP_011518679.1 | |
XM_011520378.2 | 2463 | Missense Mutation | TGG,TGT | W,C 751 | XP_011518680.1 | |
XM_011520379.2 | 2463 | Missense Mutation | TGG,TGT | W,C 751 | XP_011518681.1 | |
XM_011520381.2 | 2463 | Missense Mutation | TGG,TGT | W,C 742 | XP_011518683.1 | |
XM_017018331.1 | 2463 | Intron | XP_016873820.1 | |||
XM_017018332.1 | 2463 | Missense Mutation | TGG,TGT | W,C 811 | XP_016873821.1 | |
XM_017018333.1 | 2463 | Intron | XP_016873822.1 |