Product Details

SNP ID

rs28370433

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:1877885 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGATTTAAAGTACTCTGTTGTGACC[A/G]GGTACTATTACAGTTTATCTGTGAT

Phenotype

MIM: 602952

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

WHSC1 PubMed Links

Additional Information

For this assay, SNP(s) [rs116664822] 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

WHSC1

Gene Name

Wolf-Hirschhorn syndrome candidate 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001042424.2		Intron			NP_001035889.1
NM_007331.1		Intron			NP_015627.1
NM_133330.2		Intron			NP_579877.1
NM_133331.2		Intron			NP_579878.1
NM_133334.2		Intron			NP_579889.1
NM_133335.3		Intron			NP_579890.1
XM_005248001.3		Intron			XP_005248058.1
XM_005248002.2		Intron			XP_005248059.1
XM_005248005.2		Intron			XP_005248062.1
XM_006713914.3		Intron			XP_006713977.1
XM_011513557.2		Intron			XP_011511859.1
XM_011513560.2		Intron			XP_011511862.1
XM_017008587.1		Intron			XP_016864076.1
XM_017008588.1		Intron			XP_016864077.1

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