Product Details

SNP ID

rs201726347

Assay Type

Functionally tested

NCBI dbSNP Submissions

5

Location

Chr.1:247300802 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGATGCCGCCTGCTCTCTCTTCTCC[A/G]CCGGCTGGAGTCTGTCCGGCTGCAG

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	3437	Missense Mutation	GCG,GTG	A530V	XP_005273385.1
XM_005273330.3	3437	Missense Mutation	GCG,GTG	A494V	XP_005273387.1
XM_006711838.2	3437	Intron			XP_006711901.1
XM_011544310.1	3437	Missense Mutation	GCG,GTG	A561V	XP_011542612.1
XM_011544312.1	3437	Missense Mutation	GCG,GTG	A525V	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	A592V	XP_016858075.1
XM_017002587.1	3437	Missense Mutation	GCG,GTG	A572V	XP_016858076.1
XM_017002588.1	3437	Missense Mutation	GCG,GTG	A561V	XP_016858077.1
XM_017002589.1	3437	Missense Mutation	GCG,GTG	A556V	XP_016858078.1
XM_017002590.1	3437	Missense Mutation	GCG,GTG	A525V	XP_016858079.1
XM_017002591.1	3437	Missense Mutation	GCG,GTG	A474V	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	A297V	XP_016858083.1

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