Product Details

SNP ID

rs180994996

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:37413885 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCAGTATGAATTCTTTGATGTCTA[A/G]TGAGATTTGACATTTTAATGAAAGC

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	914	Missense Mutation	ACT,ATT	T258I	NP_689697.2
XM_006723046.2	914	Missense Mutation	ACT,ATT	T282I	XP_006723109.1
XM_006723047.3	914	Missense Mutation	ACT,ATT	T282I	XP_006723110.1
XM_006723048.3	914	Missense Mutation	ACT,ATT	T282I	XP_006723111.1
XM_011526538.2	914	Missense Mutation	ACT,ATT	T282I	XP_011524840.1
XM_011526539.2	914	Missense Mutation	ACT,ATT	T258I	XP_011524841.1
XM_017026376.1	914	Missense Mutation	ACT,ATT	T258I	XP_016881865.1
XM_017026377.1	914	Missense Mutation	ACT,ATT	T258I	XP_016881866.1
XM_017026378.1	914	Missense Mutation	ACT,ATT	T222I	XP_016881867.1
XM_017026379.1	914	Missense Mutation	ACT,ATT	T99I	XP_016881868.1
XM_017026380.1	914	Missense Mutation	ACT,ATT	T99I	XP_016881869.1
XM_017026381.1	914	Missense Mutation	ACT,ATT	T99I	XP_016881870.1
XM_017026382.1	914	Missense Mutation	ACT,ATT	T99I	XP_016881871.1

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