Product Details

SNP ID
rs72707294
Assay Type
Functionally tested
NCBI dbSNP Submissions
30
Location
Chr.1:179043812 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCACCAGCTCTCCTTAATACATGAG[C/G]AAGAGTGGGTCAGGGGAGAAGGAAA
Phenotype
MIM: 611063
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
FAM20B PubMed Links

Gene Details

Gene
FAM20B
Gene Name
family with sequence similarity 20 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001324310.1 153 UTR 5 NP_001311239.1
NM_001324311.1 153 UTR 5 NP_001311240.1
NM_014864.3 153 UTR 5 NP_055679.1
XM_017003001.1 153 UTR 5 XP_016858490.1
XM_017003002.1 153 UTR 5 XP_016858491.1

View Full Product Details