Product Details

SNP ID

rs11545619

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:52613390 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGGTTTCTCTCCAGTATGGATTCTG[T/C]GATGTTGTACAAGATGTGAATTTTG

Phenotype

MIM: 194558

Polymorphism

T/C, Transition Substitution

Allele Nomenclature

Literature Links

LOC107983997 PubMed Links

Additional Information

For this assay, SNP(s) [rs568637119] are located under a probe 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

LOC107983997

Gene Name

zinc finger protein 816-like

There are no transcripts associated with this gene.

Gene

ZNF701

Gene Name

zinc finger protein 701

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001172655.1	1756	Intron			NP_001166126.1
NM_018260.2	1756	Intron			NP_060730.2
XM_011527092.1	1756	Intron			XP_011525394.1

Gene

ZNF83

Gene Name

zinc finger protein 83

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001105549.1	1756	Intron			NP_001099019.1
NM_001105550.1	1756	Intron			NP_001099020.1
NM_001105551.1	1756	Intron			NP_001099021.1
NM_001105552.1	1756	Intron			NP_001099022.1
NM_001277945.1	1756	Missense Mutation	CAC,CGC	H392R	NP_001264874.1
NM_001277946.1	1756	Missense Mutation	CAC,CGC	H392R	NP_001264875.1
NM_001277947.1	1756	Missense Mutation	CAC,CGC	H392R	NP_001264876.1
NM_001277948.1	1756	Missense Mutation	CAC,CGC	H392R	NP_001264877.1
NM_001277949.1	1756	Missense Mutation	CAC,CGC	H392R	NP_001264878.1
NM_001277951.1	1756	Intron			NP_001264880.1
NM_001277952.1	1756	Intron			NP_001264881.1
NM_018300.3	1756	Intron			NP_060770.3
XM_017026951.1	1756	Missense Mutation	CAC,CGC	H392R	XP_016882440.1

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