Product Details

SNP ID

rs201479981

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:37414142 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATGGGATGAGCTATTACCATATGA[A/T]TTCACAGGTTCATTATATTCACAAT

Phenotype

MIM: 613904

Polymorphism

A/T, Transversion 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	657	Missense Mutation	AAA,AAT	K172N	NP_689697.2
XM_006723046.2	657	Missense Mutation	AAA,AAT	K196N	XP_006723109.1
XM_006723047.3	657	Missense Mutation	AAA,AAT	K196N	XP_006723110.1
XM_006723048.3	657	Missense Mutation	AAA,AAT	K196N	XP_006723111.1
XM_011526538.2	657	Missense Mutation	AAA,AAT	K196N	XP_011524840.1
XM_011526539.2	657	Missense Mutation	AAA,AAT	K172N	XP_011524841.1
XM_017026376.1	657	Missense Mutation	AAA,AAT	K172N	XP_016881865.1
XM_017026377.1	657	Missense Mutation	AAA,AAT	K172N	XP_016881866.1
XM_017026378.1	657	Missense Mutation	AAA,AAT	K136N	XP_016881867.1
XM_017026379.1	657	Missense Mutation	AAA,AAT	K13N	XP_016881868.1
XM_017026380.1	657	Missense Mutation	AAA,AAT	K13N	XP_016881869.1
XM_017026381.1	657	Missense Mutation	AAA,AAT	K13N	XP_016881870.1
XM_017026382.1	657	Missense Mutation	AAA,AAT	K13N	XP_016881871.1

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