Product Details

SNP ID
rs61622719
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:4419816 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGGCTACGCAGGCTGCCTCCCATT[C/G]GTGTGCACTGTTTCCTTTTTCAGCT
Phenotype
MIM: 607645 MIM: 606046
Polymorphism
C/G, 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 1382 Intron NP_001035190.1
NM_001287763.1 1382 Intron NP_001274692.1
NM_001287764.1 1382 Intron NP_001274693.1
NM_014392.4 1382 Intron NP_055207.1
XM_017008022.1 1382 Intron XP_016863511.1
Gene
STX18
Gene Name
syntaxin 18
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_016930.2 1382 UTR 3 NP_058626.1
XM_011513480.1 1382 UTR 3 XP_011511782.1
XM_011513483.1 1382 UTR 3 XP_011511785.1
XM_011513485.2 1382 UTR 3 XP_011511787.1
XM_017008296.1 1382 Intron XP_016863785.1
XM_017008297.1 1382 UTR 3 XP_016863786.1
XM_017008298.1 1382 Intron XP_016863787.1

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