Product Details

SNP ID
rs1478211
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:53838850 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AGTCCTAAAGTCTTAGAATTTTATG[C/G]AGGAGAGAGAGTTGGTTAAAATTTA
Phenotype
MIM: 614568
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
UNC13C PubMed Links

Gene Details

Gene
UNC13C
Gene Name
unc-13 homolog C
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
XM_005254394.4 Intron XP_005254451.1
XM_017022220.1 Intron XP_016877709.1
XM_017022221.1 Intron XP_016877710.1
XM_017022222.1 Intron XP_016877711.1
XM_017022223.1 Intron XP_016877712.1
XM_017022224.1 Intron XP_016877713.1
XM_017022225.1 Intron XP_016877714.1

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