Product Details

SNP ID
rs140066549
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.20:11890829 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGCTCGCTCCCGCAGAGCGTGCCCT[A/G]CGTGCGGGTGCCCGCCGAGCCCGCC
Phenotype
MIM: 615566
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
BTBD3 PubMed Links

Gene Details

Gene
BTBD3
Gene Name
BTB domain containing 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001282550.1 107 Intron NP_001269479.1
NM_001282551.1 107 Intron NP_001269480.1
NM_001282552.2 107 UTR 5 NP_001269481.1
NM_001282554.1 107 Intron NP_001269483.1
NM_014962.3 107 Intron NP_055777.1
NM_181443.3 107 Missense Mutation TAC,TGC Y21C NP_852108.2
XM_017027728.1 107 UTR 5 XP_016883217.1
XM_017027729.1 107 Intron XP_016883218.1
XM_017027730.1 107 Intron XP_016883219.1

View Full Product Details