Product Details

SNP ID
rs17011714
Assay Type
Functionally tested
NCBI dbSNP Submissions
48
Location
Chr.1:222748826 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GGTAGAATGAGTCAGAGGAATCAGA[A/C]AGTCCTATAATTCAGGGGTAAGAGA
Phenotype
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
FAM177B PubMed Links

Gene Details

Gene
FAM177B
Gene Name
family with sequence similarity 177 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001324080.1 Intron NP_001311009.1
NM_207468.2 Intron NP_997351.2
XM_017001279.1 Intron XP_016856768.1
XM_017001280.1 Intron XP_016856769.1
XM_017001281.1 Intron XP_016856770.1
XM_017001282.1 Intron XP_016856771.1
XM_017001283.1 Intron XP_016856772.1
XM_017001284.1 Intron XP_016856773.1
XM_017001285.1 Intron XP_016856774.1

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