Product Details

SNP ID: rs104893854
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:4860357 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGGATGCAGAGCCCCCGCTTCTCCC[A/C]GCCGCCGGCCAGTGAGTAGCCAGAA
Phenotype: MIM: 142983
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: LINC01396 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_002448.3	693	Missense Mutation	CAG,CCG	Q153P	NP_002439.2