Product Details

SNP ID

rs149823258

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:37413625 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGTTTTTCTCCTGTATGACTTCTCA[C/T]ATGAAGAGCAAGGGATGCAATTCGA

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	1174	Missense Mutation	ATG,GTG	M345V	NP_689697.2
XM_006723046.2	1174	Missense Mutation	ATG,GTG	M369V	XP_006723109.1
XM_006723047.3	1174	Missense Mutation	ATG,GTG	M369V	XP_006723110.1
XM_006723048.3	1174	Missense Mutation	ATG,GTG	M369V	XP_006723111.1
XM_011526538.2	1174	Missense Mutation	ATG,GTG	M369V	XP_011524840.1
XM_011526539.2	1174	Missense Mutation	ATG,GTG	M345V	XP_011524841.1
XM_017026376.1	1174	Missense Mutation	ATG,GTG	M345V	XP_016881865.1
XM_017026377.1	1174	Missense Mutation	ATG,GTG	M345V	XP_016881866.1
XM_017026378.1	1174	Missense Mutation	ATG,GTG	M309V	XP_016881867.1
XM_017026379.1	1174	Missense Mutation	ATG,GTG	M186V	XP_016881868.1
XM_017026380.1	1174	Missense Mutation	ATG,GTG	M186V	XP_016881869.1
XM_017026381.1	1174	Missense Mutation	ATG,GTG	M186V	XP_016881870.1
XM_017026382.1	1174	Missense Mutation	ATG,GTG	M186V	XP_016881871.1

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