Product Details

SNP ID
rs6672211
Assay Type
Functionally tested
NCBI dbSNP Submissions
35
Location
Chr.1:224238527 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AACTGCATAAATTATACATCTGTTA[A/G]TTGCTATCACTAAATAAAATGGACA
Phenotype
MIM: 602426
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
NVL PubMed Links

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

View Full Product Details