Product Details

SNP ID: rs146198049
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.13:112069978 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTGCGCCACAGTTTGGTCCAGAGGA[C/G]GGAGGAGGAAGGGAAGACCCCAGTG
Phenotype: MIM: 602148
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: LINC00403 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_005986.2	2380	UTR 3			NP_005977.2