Product Details

SNP ID: rs114603834
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.16:70383206 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GGAGCTTACCTTTTCTTTATCCACT[C/T]GAAGGAAGGACTTCACTGGGGCGTA
Phenotype: MIM: 607188
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: DDX19A 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_006927.3	1886	Missense Mutation	CAA,CGA	Q248R	NP_008858.1