Product Details

SNP ID

rs10799551

Assay Type

Validated

NCBI dbSNP Submissions

70

Location

Chr.1:224239469 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

CTATGGTGGTGGGGCTGCCACATTA[T/G]GTAGGAGCCCTTGTTAGGTGCTTTC

Phenotype

MIM: 602426

Polymorphism

T/G, Transversion Substitution

Allele Nomenclature

Literature Links

NVL PubMed Links

Additional Information

For this assay, SNP(s) [rs76962725] 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

NVL

Gene Name

nuclear VCP-like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001243146.1		Intron			NP_001230075.1
NM_001243147.1		Intron			NP_001230076.1
NM_002533.3		Intron			NP_002524.2
NM_206840.2		Intron			NP_996671.1
XM_011544196.1		Intron			XP_011542498.1
XM_011544198.1		Intron			XP_011542500.1
XM_011544199.1		Intron			XP_011542501.1
XM_011544200.1		Intron			XP_011542502.1
XM_017001378.1		Intron			XP_016856867.1
XM_017001379.1		Intron			XP_016856868.1
XM_017001380.1		Intron			XP_016856869.1
XM_017001381.1		Intron			XP_016856870.1
XM_017001382.1		Intron			XP_016856871.1
XM_017001383.1		Intron			XP_016856872.1
XM_017001384.1		Intron			XP_016856873.1
XM_017001385.1		Intron			XP_016856874.1
XM_017001386.1		Intron			XP_016856875.1

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