Product Details

SNP ID
rs62119681
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:39348314 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTAGGTGTTTTTGGAAGAGCTGCAG[C/G]CTTTGAAGAAACATCTCTTGATGAT
Phenotype
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
SAMD4B PubMed Links

Gene Details

Gene
SAMD4B
Gene Name
sterile alpha motif domain containing 4B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001303614.1 5530 Intron NP_001290543.1
NM_018028.3 5530 UTR 5 NP_060498.2
XM_011527057.2 5530 Intron XP_011525359.1
XM_011527060.2 5530 Intron XP_011525362.1
XM_011527061.2 5530 Intron XP_011525363.1
XM_011527062.2 5530 Intron XP_011525364.1
XM_011527063.2 5530 Intron XP_011525365.1
XM_011527064.2 5530 Intron XP_011525366.1
XM_017026918.1 5530 Intron XP_016882407.1
XM_017026919.1 5530 UTR 5 XP_016882408.1
XM_017026920.1 5530 Intron XP_016882409.1
XM_017026921.1 5530 Intron XP_016882410.1
XM_017026922.1 5530 Intron XP_016882411.1
XM_017026923.1 5530 UTR 5 XP_016882412.1

View Full Product Details