Product Details

SNP ID
rs150299026
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:96886365 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCAATGAGACGCCATTCTGGTTAC[A/G]ATTCGAGGGCCGAAGCTCTTTCTTG
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
FAM178B PubMed Links

Gene Details

Gene
FAM178B
Gene Name
family with sequence similarity 178 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001122646.2 Intron NP_001116118.2
NM_001172667.1 Intron NP_001166138.1
NM_016490.4 Intron NP_057574.2
XM_011511294.2 Intron XP_011509596.1
XM_011511297.2 Intron XP_011509599.1
XM_017004263.1 Intron XP_016859752.1
XM_017004264.1 Intron XP_016859753.1
XM_017004265.1 Intron XP_016859754.1
XM_017004266.1 Intron XP_016859755.1
XM_017004267.1 Intron XP_016859756.1
XM_017004268.1 Intron XP_016859757.1

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