Product Details

SNP ID

rs13090196

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:149038147 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TAATCCTAGAACTCCTAAGTCTCTA[C/G]GTTGAATGCAAAGGAAATTGCATTT

Phenotype

MIM: 603257

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

HLTF PubMed Links

Additional Information

For this assay, SNP(s) [rs79393620] 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

HLTF

Gene Name

helicase like transcription factor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001318934.1		Intron			NP_001305863.1
NM_001318935.1		Intron			NP_001305864.1
NM_003071.3		Intron			NP_003062.2
NM_139048.2		Intron			NP_620636.1
XM_011513091.1		Intron			XP_011511393.1
XM_011513092.1		Intron			XP_011511394.1
XM_011513093.1		Intron			XP_011511395.1
XM_017007078.1		Intron			XP_016862567.1
XM_017007079.1		Intron			XP_016862568.1

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