Product Details

SNP ID
rs138795649
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:4387665 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGGGAACAATTTCGCAGAGAAGGG[C/T]ACCAAGCAGCCGCTGCTGGAGGATG
Phenotype
MIM: 607645
Polymorphism
C/T, Transition 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_001040101.1 273 Silent Mutation GGC,GGT G12G NP_001035190.1
NM_001287763.1 273 Silent Mutation GGC,GGT G12G NP_001274692.1
NM_001287764.1 273 UTR 5 NP_001274693.1
NM_014392.4 273 Silent Mutation GGC,GGT G12G NP_055207.1
XM_017008022.1 273 Silent Mutation GGC,GGT G12G XP_016863511.1

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