Product Details

SNP ID

rs139933067

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:37413550 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTGTATGAATTCTAACATGTATAA[G/T]AAGCATGGAAAACTGAGAGAAGGCT

Phenotype

MIM: 613904

Polymorphism

G/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	1249	Missense Mutation	ATT,CTT	I370L	NP_689697.2
XM_006723046.2	1249	Missense Mutation	ATT,CTT	I394L	XP_006723109.1
XM_006723047.3	1249	Missense Mutation	ATT,CTT	I394L	XP_006723110.1
XM_006723048.3	1249	Missense Mutation	ATT,CTT	I394L	XP_006723111.1
XM_011526538.2	1249	Missense Mutation	ATT,CTT	I394L	XP_011524840.1
XM_011526539.2	1249	Missense Mutation	ATT,CTT	I370L	XP_011524841.1
XM_017026376.1	1249	Missense Mutation	ATT,CTT	I370L	XP_016881865.1
XM_017026377.1	1249	Missense Mutation	ATT,CTT	I370L	XP_016881866.1
XM_017026378.1	1249	Missense Mutation	ATT,CTT	I334L	XP_016881867.1
XM_017026379.1	1249	Missense Mutation	ATT,CTT	I211L	XP_016881868.1
XM_017026380.1	1249	Missense Mutation	ATT,CTT	I211L	XP_016881869.1
XM_017026381.1	1249	Missense Mutation	ATT,CTT	I211L	XP_016881870.1
XM_017026382.1	1249	Missense Mutation	ATT,CTT	I211L	XP_016881871.1

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