Product Details

SNP ID
rs148710392
Assay Type
Functionally tested
NCBI dbSNP Submissions
7
Location
Chr.1:26415359 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGTTTGGTGTTAGGGTTGCGGGGGC[A/G]GGTGGGGAAATATACGGAATCTTTC
Phenotype
MIM: 611043
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
LIN28A PubMed Links

Gene Details

Gene
LIN28A
Gene Name
lin-28 homolog A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_024674.5 Intron NP_078950.1
XM_011542148.1 Intron XP_011540450.1

View Full Product Details