Product Details

SNP ID
rs148958456
Assay Type
Functionally tested
NCBI dbSNP Submissions
5
Location
Chr.1:247300645 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACTGGAAGGGCCGGGCTTTGTCCTT[C/T]AGGTGAAAGTGGCTGCGGTGCCGAG
Phenotype
MIM: 613911
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
ZNF496 PubMed Links

Gene Details

Gene
ZNF496
Gene Name
zinc finger protein 496
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
XM_005273328.3 3594 Silent Mutation CTA,CTG L582L XP_005273385.1
XM_005273330.3 3594 Silent Mutation CTA,CTG L546L XP_005273387.1
XM_006711838.2 3594 Intron XP_006711901.1
XM_011544310.1 3594 Silent Mutation CTA,CTG L613L XP_011542612.1
XM_011544312.1 3594 Silent Mutation CTA,CTG L577L XP_011542614.1
XM_011544314.2 3594 Intron XP_011542616.1
XM_011544315.2 3594 Intron XP_011542617.1
XM_011544316.1 3594 Intron XP_011542618.1
XM_017002586.1 3594 Silent Mutation CTA,CTG L644L XP_016858075.1
XM_017002587.1 3594 Silent Mutation CTA,CTG L624L XP_016858076.1
XM_017002588.1 3594 Silent Mutation CTA,CTG L613L XP_016858077.1
XM_017002589.1 3594 Silent Mutation CTA,CTG L608L XP_016858078.1
XM_017002590.1 3594 Silent Mutation CTA,CTG L577L XP_016858079.1
XM_017002591.1 3594 Silent Mutation CTA,CTG L526L XP_016858080.1
XM_017002592.1 3594 Intron XP_016858081.1
XM_017002593.1 3594 Intron XP_016858082.1
XM_017002594.1 3594 Silent Mutation CTA,CTG L349L XP_016858083.1

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