Product Details

SNP ID: rs184583395
Assay Type: Functionally tested
NCBI dbSNP Submissions: 5
Location: Chr.1:28553707 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GCCACCATGGGGGAGACCGTAATGA[A/G]CGTCAAAATTATCCGAAACCGCCTC
Phenotype
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: TRNAU1AP PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_017846.4	189	Missense Mutation	AAC,AGC	N32S	NP_060316.1
XM_017001542.1	189	Intron			XP_016857031.1