Product Details

SNP ID: rs191774490
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.16:56609270 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCTCCTGTCTGCCCCCAGGCTGCTG[C/T]TCCTGCTGCCCTGTGGGCTGTGCCA
Phenotype: MIM: 156358 MIM: 156360
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: MT1L PubMed Links

Gene Details

There are no transcripts associated with this gene.

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005953.3	192	Silent Mutation			NP_005944.1