Product Details

SNP ID
rs114501214
Assay Type
Functionally Tested
NCBI dbSNP Submissions
10
Location
Chr.1:204837731 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCAGTGATGCTGCACTGGAAAGTAA[C/T]GCCGGGGAATGCTTACAACCAGCCA
Phenotype
MIM: 609145
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
NFASC PubMed Links

Gene Details

Gene
NFASC
Gene Name
neurofascin
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001005388.2 Intron NP_001005388.2
NM_001005389.1 Intron NP_001005389.2
NM_001160331.1 Intron NP_001153803.1
NM_001160332.1 Intron NP_001153804.1
NM_001160333.1 Intron NP_001153805.1
NM_015090.3 Intron NP_055905.2
XM_005244989.3 Intron XP_005245046.2
XM_005244991.3 Intron XP_005245048.2
XM_005244992.4 Intron XP_005245049.2
XM_005244993.3 Intron XP_005245050.2
XM_005244997.3 Intron XP_005245054.2
XM_011509311.1 Intron XP_011507613.1
XM_011509312.1 Intron XP_011507614.1
XM_011509313.1 Intron XP_011507615.1
XM_011509314.1 Intron XP_011507616.1
XM_011509315.1 Intron XP_011507617.1
XM_011509316.1 Intron XP_011507618.1
XM_011509317.1 Intron XP_011507619.1
XM_011509318.2 Intron XP_011507620.1
XM_011509319.1 Intron XP_011507621.1
XM_011509320.2 Intron XP_011507622.1
XM_011509321.1 Intron XP_011507623.1
XM_011509322.1 Intron XP_011507624.1
XM_011509323.1 Intron XP_011507625.1
XM_011509324.1 Intron XP_011507626.1
XM_011509325.1 Intron XP_011507627.1
XM_011509326.1 Intron XP_011507628.1
XM_011509327.1 Intron XP_011507629.1
XM_011509328.1 Intron XP_011507630.1
XM_017000733.1 Intron XP_016856222.1
XM_017000734.1 Intron XP_016856223.1
XM_017000735.1 Intron XP_016856224.1
XM_017000736.1 Intron XP_016856225.1
XM_017000737.1 Intron XP_016856226.1
XM_017000738.1 Intron XP_016856227.1
XM_017000739.1 Intron XP_016856228.1
XM_017000740.1 Intron XP_016856229.1
XM_017000741.1 Intron XP_016856230.1
XM_017000742.1 Intron XP_016856231.1
XM_017000743.1 Intron XP_016856232.1

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