Product Details

SNP ID
rs4490411
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:4385724 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGGAGAGTTGGGGCGAGTTACGAGA[G/T]ACCCACTAGGTCACCTGTCAAAGAC
Phenotype
MIM: 607645
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
NSG1 PubMed Links

Gene Details

Gene
NSG1
Gene Name
neuron specific gene family member 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001040101.1 Intron NP_001035190.1
NM_001287763.1 Intron NP_001274692.1
NM_001287764.1 Intron NP_001274693.1
NM_014392.4 Intron NP_055207.1
XM_017008022.1 Intron XP_016863511.1

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