Product Details

SNP ID

rs111413551

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:36183415 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCACCAGTGTGAATTTTCTGATGT[C/T]GAATAAGGTGTGAGCCACGGCTAAA

Phenotype

MIM: 614275

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

ZNF565 PubMed Links

Additional Information

For this assay, SNP(s) [rs61741493] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

ZNF565

Gene Name

zinc finger protein 565

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001042474.2	1356	Missense Mutation	CAA,CGA	Q184R	NP_001035939.1
NM_152477.4	1356	Missense Mutation	CAA,CGA	Q184R	NP_689690.3
XM_011526512.2	1356	Missense Mutation	CAA,CGA	Q184R	XP_011524814.1
XM_011526514.2	1356	Missense Mutation	CAA,CGA	Q184R	XP_011524816.1
XM_017026341.1	1356	Missense Mutation	CAA,CGA	Q184R	XP_016881830.1
XM_017026342.1	1356	Missense Mutation	CAA,CGA	Q119R	XP_016881831.1
XM_017026343.1	1356	Missense Mutation	CAA,CGA	Q119R	XP_016881832.1

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