Product Details

SNP ID

rs150159350

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:37412854 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTATTACATTCATAGGGTTTTTCAC[C/T]TGTATGGCCTCTCATGTGCACAATA

Phenotype

MIM: 613904

Polymorphism

C/T, 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	1945	Missense Mutation	AGT,GGT	S602G	NP_689697.2
XM_006723046.2	1945	Missense Mutation	AGT,GGT	S626G	XP_006723109.1
XM_006723047.3	1945	Missense Mutation	AGT,GGT	S626G	XP_006723110.1
XM_006723048.3	1945	Missense Mutation	AGT,GGT	S626G	XP_006723111.1
XM_011526538.2	1945	Missense Mutation	AGT,GGT	S626G	XP_011524840.1
XM_011526539.2	1945	Missense Mutation	AGT,GGT	S602G	XP_011524841.1
XM_017026376.1	1945	Missense Mutation	AGT,GGT	S602G	XP_016881865.1
XM_017026377.1	1945	Missense Mutation	AGT,GGT	S602G	XP_016881866.1
XM_017026378.1	1945	Missense Mutation	AGT,GGT	S566G	XP_016881867.1
XM_017026379.1	1945	Missense Mutation	AGT,GGT	S443G	XP_016881868.1
XM_017026380.1	1945	Missense Mutation	AGT,GGT	S443G	XP_016881869.1
XM_017026381.1	1945	Missense Mutation	AGT,GGT	S443G	XP_016881870.1
XM_017026382.1	1945	Missense Mutation	AGT,GGT	S443G	XP_016881871.1

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