Product Details

SNP ID
rs14361
Assay Type
Functionally Tested
NCBI dbSNP Submissions
5
Location
Chr.1:92834819 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATAGAGGGGGATATGATAGTCTGCG[C/T]AGCGTATGCACACGAACTGCCAAAA
Phenotype
MIM: 614542 MIM: 603634 MIM: 603635
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
FAM69A PubMed Links
Additional Information
For this assay, SNP(s) [rs113792800] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene
FAM69A
Gene Name
family with sequence similarity 69 member A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001006605.4 308 Intron NP_001006606.2
NM_001252269.1 308 Intron NP_001239198.1
NM_001252270.1 308 Intron NP_001239199.1
NM_001252271.1 308 Intron NP_001239200.1
NM_001252273.1 308 Intron NP_001239202.1
Gene
RPL5
Gene Name
ribosomal protein L5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000969.3 308 Missense Mutation NP_000960.2
Gene
SNORA66
Gene Name
small nucleolar RNA, H/ACA box 66
There are no transcripts associated with this gene.

Gene
SNORD21
Gene Name
small nucleolar RNA, C/D box 21
There are no transcripts associated with this gene.

View Full Product Details