Product Details

SNP ID

rs143361188

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:37413725 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAACTTTCTGATGTGCAATGAGGCT[C/T]TGCTTCTGGCTGAATGCTTTTCCAC

Phenotype

MIM: 613904

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

ZNF569 PubMed Links

Gene Details

Gene

ZNF569

Gene Name

zinc finger protein 569

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152484.2	1074	Silent Mutation	CAA,CAG	Q311Q	NP_689697.2
XM_006723046.2	1074	Silent Mutation	CAA,CAG	Q335Q	XP_006723109.1
XM_006723047.3	1074	Silent Mutation	CAA,CAG	Q335Q	XP_006723110.1
XM_006723048.3	1074	Silent Mutation	CAA,CAG	Q335Q	XP_006723111.1
XM_011526538.2	1074	Silent Mutation	CAA,CAG	Q335Q	XP_011524840.1
XM_011526539.2	1074	Silent Mutation	CAA,CAG	Q311Q	XP_011524841.1
XM_017026376.1	1074	Silent Mutation	CAA,CAG	Q311Q	XP_016881865.1
XM_017026377.1	1074	Silent Mutation	CAA,CAG	Q311Q	XP_016881866.1
XM_017026378.1	1074	Silent Mutation	CAA,CAG	Q275Q	XP_016881867.1
XM_017026379.1	1074	Silent Mutation	CAA,CAG	Q152Q	XP_016881868.1
XM_017026380.1	1074	Silent Mutation	CAA,CAG	Q152Q	XP_016881869.1
XM_017026381.1	1074	Silent Mutation	CAA,CAG	Q152Q	XP_016881870.1
XM_017026382.1	1074	Silent Mutation	CAA,CAG	Q152Q	XP_016881871.1

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