Product Details

SNP ID

rs116719577

Assay Type

Functionally tested

NCBI dbSNP Submissions

8

Location

Chr.1:26411441 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCGAGGAGGCGCCGGAGGACGCGGC[C/G]CGGGCGGCGGACGAGCCTCAGCTGC

Phenotype

MIM: 611043

Polymorphism

C/G, Transversion 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

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