Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGATGCCGCCTGCTCTCTCTTCTCC[A/G]CCGGCTGGAGTCTGTCCGGCTGCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
MIM: 613911 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZNF496 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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ZNF496 - zinc finger protein 496 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_005273328.3 | 3437 | Missense Mutation | GCG,GTG | A,V 530 | XP_005273385.1 | |
XM_005273330.3 | 3437 | Missense Mutation | GCG,GTG | A,V 494 | XP_005273387.1 | |
XM_006711838.2 | 3437 | Intron | XP_006711901.1 | |||
XM_011544310.1 | 3437 | Missense Mutation | GCG,GTG | A,V 561 | XP_011542612.1 | |
XM_011544312.1 | 3437 | Missense Mutation | GCG,GTG | A,V 525 | XP_011542614.1 | |
XM_011544314.2 | 3437 | Intron | XP_011542616.1 | |||
XM_011544315.2 | 3437 | Intron | XP_011542617.1 | |||
XM_011544316.1 | 3437 | Intron | XP_011542618.1 | |||
XM_017002586.1 | 3437 | Missense Mutation | GCG,GTG | A,V 592 | XP_016858075.1 | |
XM_017002587.1 | 3437 | Missense Mutation | GCG,GTG | A,V 572 | XP_016858076.1 | |
XM_017002588.1 | 3437 | Missense Mutation | GCG,GTG | A,V 561 | XP_016858077.1 | |
XM_017002589.1 | 3437 | Missense Mutation | GCG,GTG | A,V 556 | XP_016858078.1 | |
XM_017002590.1 | 3437 | Missense Mutation | GCG,GTG | A,V 525 | XP_016858079.1 | |
XM_017002591.1 | 3437 | Missense Mutation | GCG,GTG | A,V 474 | XP_016858080.1 | |
XM_017002592.1 | 3437 | Intron | XP_016858081.1 | |||
XM_017002593.1 | 3437 | Intron | XP_016858082.1 | |||
XM_017002594.1 | 3437 | Missense Mutation | GCG,GTG | A,V 297 | XP_016858083.1 |