Product Details

SNP ID: rs146627322
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.16:70380026 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CATAATTGCATTGCTTTTCATCAAC[A/T]CTCAAAACAGCCTCTTCAGGAAGCA
Phenotype: MIM: 607188
Polymorphism: A/T, Transversion 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	3859	UTR 3			NP_008858.1