Product Details

SNP ID

rs1742236

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.10:37763371 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ATAACTTCAAGGAGCCTGGCTCCAG[C/G]GAGTGATCTCCCTAAGCAAACCTTT

Phenotype

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

ZNF248 PubMed Links

Additional Information

For this assay, SNP(s) [rs117771731] 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

ZNF248

Gene Name

zinc finger protein 248

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001267597.1		Intron			NP_001254526.1
NM_001267605.1		Intron			NP_001254534.1
NM_001267606.1		Intron			NP_001254535.1
NM_001267607.1		Intron			NP_001254536.1
NM_021045.2		Intron			NP_066383.1
XM_006717485.3		Intron			XP_006717548.1
XM_011519597.2		Intron			XP_011517899.1
XM_011519598.2		Intron			XP_011517900.1
XM_011519599.1		Intron			XP_011517901.1
XM_011519600.2		Intron			XP_011517902.1
XM_017016444.1		Intron			XP_016871933.1
XM_017016445.1		Intron			XP_016871934.1
XM_017016446.1		Intron			XP_016871935.1
XM_017016447.1		Intron			XP_016871936.1
XM_017016448.1		Intron			XP_016871937.1
XM_017016449.1		Intron			XP_016871938.1
XM_017016450.1		Intron			XP_016871939.1
XM_017016451.1		Intron			XP_016871940.1

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