Product Details

SNP ID

rs202186412

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:37413948 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTACATTTGTAAGACTGCTCCCTA[C/G]TGTGAATTTTATAATGTTTAATAAG

Phenotype

MIM: 613904

Polymorphism

C/G, 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	851	Missense Mutation	ACT,AGT	T237S	NP_689697.2
XM_006723046.2	851	Missense Mutation	ACT,AGT	T261S	XP_006723109.1
XM_006723047.3	851	Missense Mutation	ACT,AGT	T261S	XP_006723110.1
XM_006723048.3	851	Missense Mutation	ACT,AGT	T261S	XP_006723111.1
XM_011526538.2	851	Missense Mutation	ACT,AGT	T261S	XP_011524840.1
XM_011526539.2	851	Missense Mutation	ACT,AGT	T237S	XP_011524841.1
XM_017026376.1	851	Missense Mutation	ACT,AGT	T237S	XP_016881865.1
XM_017026377.1	851	Missense Mutation	ACT,AGT	T237S	XP_016881866.1
XM_017026378.1	851	Missense Mutation	ACT,AGT	T201S	XP_016881867.1
XM_017026379.1	851	Missense Mutation	ACT,AGT	T78S	XP_016881868.1
XM_017026380.1	851	Missense Mutation	ACT,AGT	T78S	XP_016881869.1
XM_017026381.1	851	Missense Mutation	ACT,AGT	T78S	XP_016881870.1
XM_017026382.1	851	Missense Mutation	ACT,AGT	T78S	XP_016881871.1

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