Product Details

SNP ID

rs146090389

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:37413515 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTTTCCACACTCATTACATTCATA[A/G]GGTTTTTCACCTGTATGAATTCTAA

Phenotype

MIM: 613904

Polymorphism

A/G, 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	1284	Silent Mutation	CCC,CCT	P381P	NP_689697.2
XM_006723046.2	1284	Silent Mutation	CCC,CCT	P405P	XP_006723109.1
XM_006723047.3	1284	Silent Mutation	CCC,CCT	P405P	XP_006723110.1
XM_006723048.3	1284	Silent Mutation	CCC,CCT	P405P	XP_006723111.1
XM_011526538.2	1284	Silent Mutation	CCC,CCT	P405P	XP_011524840.1
XM_011526539.2	1284	Silent Mutation	CCC,CCT	P381P	XP_011524841.1
XM_017026376.1	1284	Silent Mutation	CCC,CCT	P381P	XP_016881865.1
XM_017026377.1	1284	Silent Mutation	CCC,CCT	P381P	XP_016881866.1
XM_017026378.1	1284	Silent Mutation	CCC,CCT	P345P	XP_016881867.1
XM_017026379.1	1284	Silent Mutation	CCC,CCT	P222P	XP_016881868.1
XM_017026380.1	1284	Silent Mutation	CCC,CCT	P222P	XP_016881869.1
XM_017026381.1	1284	Silent Mutation	CCC,CCT	P222P	XP_016881870.1
XM_017026382.1	1284	Silent Mutation	CCC,CCT	P222P	XP_016881871.1

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