Product Details

SNP ID
rs13346452
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:39346160 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GGCCTGCCTTCAGGGAGCTCACAAT[A/G]CCAGTAGGGGGCTTGGGCATGTACA
Phenotype
Polymorphism
A/G, Transition 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 3376 Intron NP_001290543.1
NM_018028.3 3376 Intron NP_060498.2
XM_011527057.2 3376 Intron XP_011525359.1
XM_011527060.2 3376 Intron XP_011525362.1
XM_011527061.2 3376 Intron XP_011525363.1
XM_011527062.2 3376 Intron XP_011525364.1
XM_011527063.2 3376 Intron XP_011525365.1
XM_011527064.2 3376 Intron XP_011525366.1
XM_017026918.1 3376 Intron XP_016882407.1
XM_017026919.1 3376 Intron XP_016882408.1
XM_017026920.1 3376 Intron XP_016882409.1
XM_017026921.1 3376 Intron XP_016882410.1
XM_017026922.1 3376 Intron XP_016882411.1
XM_017026923.1 3376 UTR 5 XP_016882412.1

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