Product Details

SNP ID: rs111899359
Assay Type: Functionally tested
NCBI dbSNP Submissions: 1
Location: Chr.1:183023738 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CGGGATGAGAGGGAGCCATCGGGCC[A/G]CGCCGGCCCTGCGGCCCCGGGGGCG
Phenotype: MIM: 150290
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: LAMC1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002293.3	279	Missense Mutation	ACG,GCG	T8A	NP_002284.3