Product Details

SNP ID

rs140961822

Assay Type

Functionally tested

NCBI dbSNP Submissions

4

Location

Chr.1:247300582 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGTGCAGGCGCTCGTGGCGGAGGAG[A/G]TCATAGTTCTGCGTGAAGCTCTTGA

Phenotype

MIM: 613911

Polymorphism

A/G, 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	3657	Silent Mutation	GAC,GAT	D603D	XP_005273385.1
XM_005273330.3	3657	Silent Mutation	GAC,GAT	D567D	XP_005273387.1
XM_006711838.2	3657	Intron			XP_006711901.1
XM_011544310.1	3657	Silent Mutation	GAC,GAT	D634D	XP_011542612.1
XM_011544312.1	3657	Silent Mutation	GAC,GAT	D598D	XP_011542614.1
XM_011544314.2	3657	Intron			XP_011542616.1
XM_011544315.2	3657	Intron			XP_011542617.1
XM_011544316.1	3657	Intron			XP_011542618.1
XM_017002586.1	3657	Silent Mutation	GAC,GAT	D665D	XP_016858075.1
XM_017002587.1	3657	Silent Mutation	GAC,GAT	D645D	XP_016858076.1
XM_017002588.1	3657	Silent Mutation	GAC,GAT	D634D	XP_016858077.1
XM_017002589.1	3657	Silent Mutation	GAC,GAT	D629D	XP_016858078.1
XM_017002590.1	3657	Silent Mutation	GAC,GAT	D598D	XP_016858079.1
XM_017002591.1	3657	Silent Mutation	GAC,GAT	D547D	XP_016858080.1
XM_017002592.1	3657	Intron			XP_016858081.1
XM_017002593.1	3657	Intron			XP_016858082.1
XM_017002594.1	3657	Silent Mutation	GAC,GAT	D370D	XP_016858083.1

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