Product Details

SNP ID
rs4652346
Assay Type
Functionally tested
NCBI dbSNP Submissions
38
Location
Chr.1:179028024 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGCCTTAAAGTTTCTGCTTCTTAT[C/T]TCTTCTGAATTTTAAATTCCTAAAT
Phenotype
MIM: 611063
Polymorphism
C/T, Transition 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 Intron NP_001311239.1
NM_001324311.1 Intron NP_001311240.1
NM_014864.3 Intron NP_055679.1
XM_017003001.1 Intron XP_016858490.1
XM_017003002.1 Intron XP_016858491.1

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