Product Details

SNP ID
rs12565875
Assay Type
Functionally tested
NCBI dbSNP Submissions
38
Location
Chr.1:224237463 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AACTTAGAACTCTTAGAATTTCTCA[A/T]GAGACTGGATGTAGAGGAAAAAAAA
Phenotype
MIM: 602426
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
LOC101927164 PubMed Links

Gene Details

Gene
LOC101927164
Gene Name
uncharacterized LOC101927164
There are no transcripts associated with this gene.

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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