Product Details

SNP ID
rs12299127
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.12:77576379 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTCATCAATGTCAATTCACATGGAC[A/C]TGTTTTATTCTTTCTCTTTCAACTG
Phenotype
MIM: 611629
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
NAV3 PubMed Links

Gene Details

Gene
NAV3
Gene Name
neuron navigator 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001024383.1 Intron NP_001019554.1
NM_014903.5 Intron NP_055718.4
XM_005269215.3 Intron XP_005269272.1
XM_011538940.2 Intron XP_011537242.1
XM_011538941.2 Intron XP_011537243.1
XM_011538944.2 Intron XP_011537246.1
XM_017020164.1 Intron XP_016875653.1
XM_017020165.1 Intron XP_016875654.1
XM_017020166.1 Intron XP_016875655.1
XM_017020167.1 Intron XP_016875656.1
XM_017020168.1 Intron XP_016875657.1
XM_017020169.1 Intron XP_016875658.1
XM_017020170.1 Intron XP_016875659.1
XM_017020171.1 Intron XP_016875660.1
XM_017020172.1 Intron XP_016875661.1
XM_017020173.1 Intron XP_016875662.1
XM_017020174.1 Intron XP_016875663.1
XM_017020175.1 Intron XP_016875664.1

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