Product Details

SNP ID

rs9964794

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.18:12949295 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACAACTCCAGAGTAACTGGAAATCT[A/G]AAGGATAGTTTATCCTTTTTCACAT

Phenotype

MIM: 609263

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

SEH1L PubMed Links

Additional Information

For this assay, SNP(s) [rs77908530] 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

SEH1L

Gene Name

SEH1 like nucleoporin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001013437.1		Intron			NP_001013455.1
NM_031216.3		Intron			NP_112493.2
XM_005258152.4		Intron			XP_005258209.1
XM_011525742.2		Intron			XP_011524044.1
XM_011525743.2		Intron			XP_011524045.1
XM_011525744.1		Intron			XP_011524046.1
XM_011525745.2		Intron			XP_011524047.1
XM_011525746.2		Intron			XP_011524048.1
XM_017026025.1		Intron			XP_016881514.1
XM_017026026.1		Intron			XP_016881515.1
XM_017026027.1		Intron			XP_016881516.1

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