Product Details

SNP ID: rs3754822
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.2:197462590 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TAGTATCGGGAGTGGAGGATTACAA[G/A]CATTTTGTTCCTTGGTGCAAAAAAT
Phenotype
Polymorphism: G/A, Transition substitution
Allele Nomenclature
Literature Links: COQ10B PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001320818.1	488	Silent Mutation	AAA,AAG	K52K	NP_001307747.1
NM_001320819.1	488	Silent Mutation	AAA,AAG	K74K	NP_001307748.1
NM_001320820.1	488	Silent Mutation	AAA,AAG	K59K	NP_001307749.1
NM_025147.4	488	Silent Mutation	AAA,AAG	K102K	NP_079423.1