Product Details

SNP ID

rs144653466

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:149765530 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGGGAGAGGGCCTGGCCGGGCCGGC[A/C]GTCTGGTGCACCCTTTGGTGCCGCA

Phenotype

MIM: 614040

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

ZNF467 PubMed Links

Additional Information

For this assay, SNP(s) [rs6965332] 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

ZNF467

Gene Name

zinc finger protein 467

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_005249959.4	1085	Silent Mutation			XP_005250016.1
XM_005249960.4	1085	Silent Mutation			XP_005250017.1
XM_005249961.4	1085	Silent Mutation			XP_005250018.1
XM_006715864.3	1085	Silent Mutation			XP_006715927.1
XM_011515855.2	1085	Silent Mutation			XP_011514157.1
XM_011515856.2	1085	Silent Mutation			XP_011514158.1
XM_011515857.2	1085	Silent Mutation			XP_011514159.1
XM_011515858.1	1085	Silent Mutation			XP_011514160.1
XM_017011799.1	1085	Silent Mutation			XP_016867288.1

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