Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGTTTGGCCTTGCCGTTTTCCAGC[A/G]GCTCTTTGGGACCCTTGTCCGCGTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
13 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 |
---|---|---|
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 |
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 | 3491 | Missense Mutation | CCG,CTG | P,L 548 | XP_005273385.1 | |
XM_005273330.3 | 3491 | Missense Mutation | CCG,CTG | P,L 512 | XP_005273387.1 | |
XM_006711838.2 | 3491 | Intron | XP_006711901.1 | |||
XM_011544310.1 | 3491 | Missense Mutation | CCG,CTG | P,L 579 | XP_011542612.1 | |
XM_011544312.1 | 3491 | Missense Mutation | CCG,CTG | P,L 543 | XP_011542614.1 | |
XM_011544314.2 | 3491 | Intron | XP_011542616.1 | |||
XM_011544315.2 | 3491 | Intron | XP_011542617.1 | |||
XM_011544316.1 | 3491 | Intron | XP_011542618.1 | |||
XM_017002586.1 | 3491 | Missense Mutation | CCG,CTG | P,L 610 | XP_016858075.1 | |
XM_017002587.1 | 3491 | Missense Mutation | CCG,CTG | P,L 590 | XP_016858076.1 | |
XM_017002588.1 | 3491 | Missense Mutation | CCG,CTG | P,L 579 | XP_016858077.1 | |
XM_017002589.1 | 3491 | Missense Mutation | CCG,CTG | P,L 574 | XP_016858078.1 | |
XM_017002590.1 | 3491 | Missense Mutation | CCG,CTG | P,L 543 | XP_016858079.1 | |
XM_017002591.1 | 3491 | Missense Mutation | CCG,CTG | P,L 492 | XP_016858080.1 | |
XM_017002592.1 | 3491 | Intron | XP_016858081.1 | |||
XM_017002593.1 | 3491 | Intron | XP_016858082.1 | |||
XM_017002594.1 | 3491 | Missense Mutation | CCG,CTG | P,L 315 | XP_016858083.1 |