Product Details

SNP ID

rs144306949

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:37413055 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTCTCAAATGAAGGGTAAGGGATG[A/C]AATTTGAGAGAAGGCTTTACCACAT

Phenotype

MIM: 613904

Polymorphism

A/C, 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	1744	Missense Mutation	GCA,TCA	A535S	NP_689697.2
XM_006723046.2	1744	Missense Mutation	GCA,TCA	A559S	XP_006723109.1
XM_006723047.3	1744	Missense Mutation	GCA,TCA	A559S	XP_006723110.1
XM_006723048.3	1744	Missense Mutation	GCA,TCA	A559S	XP_006723111.1
XM_011526538.2	1744	Missense Mutation	GCA,TCA	A559S	XP_011524840.1
XM_011526539.2	1744	Missense Mutation	GCA,TCA	A535S	XP_011524841.1
XM_017026376.1	1744	Missense Mutation	GCA,TCA	A535S	XP_016881865.1
XM_017026377.1	1744	Missense Mutation	GCA,TCA	A535S	XP_016881866.1
XM_017026378.1	1744	Missense Mutation	GCA,TCA	A499S	XP_016881867.1
XM_017026379.1	1744	Missense Mutation	GCA,TCA	A376S	XP_016881868.1
XM_017026380.1	1744	Missense Mutation	GCA,TCA	A376S	XP_016881869.1
XM_017026381.1	1744	Missense Mutation	GCA,TCA	A376S	XP_016881870.1
XM_017026382.1	1744	Missense Mutation	GCA,TCA	A376S	XP_016881871.1

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