Product Details

SNP ID

rs137886346

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:53068811 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCCTTGCAAGTTGTGATGTTTGAG[C/T]GAAGACTTTACCACATTCATTACAC

Phenotype

MIM: 600398

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

ZNF160 PubMed Links

Additional Information

For this assay, SNP(s) [rs78382850] 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

ZNF160

Gene Name

zinc finger protein 160

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001102603.1	2135	Missense Mutation			NP_001096073.1
NM_001322125.1	2135	Intron			NP_001309054.1
NM_001322126.1	2135	Intron			NP_001309055.1
NM_001322128.1	2135	Missense Mutation			NP_001309057.1
NM_001322129.1	2135	Missense Mutation			NP_001309058.1
NM_001322130.1	2135	Missense Mutation			NP_001309059.1
NM_001322131.1	2135	Missense Mutation			NP_001309060.1
NM_001322132.1	2135	Missense Mutation			NP_001309061.1
NM_001322133.1	2135	Missense Mutation			NP_001309062.1
NM_001322134.1	2135	Missense Mutation			NP_001309063.1
NM_001322135.1	2135	Missense Mutation			NP_001309064.1
NM_001322136.1	2135	Missense Mutation			NP_001309065.1
NM_001322137.1	2135	Missense Mutation			NP_001309066.1
NM_001322138.1	2135	Missense Mutation			NP_001309067.1
NM_001322139.1	2135	Missense Mutation			NP_001309068.1
NM_033288.3	2135	Missense Mutation			NP_150630.2
NM_198893.2	2135	Missense Mutation			NP_942596.1
XM_017027445.1	2135	Missense Mutation			XP_016882934.1
XM_017027446.1	2135	Missense Mutation			XP_016882935.1
XM_017027447.1	2135	Intron			XP_016882936.1
XM_017027448.1	2135	Intron			XP_016882937.1

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