Product Details

SNP ID
rs2381409
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:35829393 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGGGGGTGGGGAGCGGAGCCGCGGG[C/T]CAGCTCTGCGAGCGCCCCGCGCTGG
Phenotype
MIM: 616888
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FAM221B PubMed Links

Gene Details

Gene
FAM221B
Gene Name
family with sequence similarity 221 member B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001012446.3 67 Intron NP_001012448.2
XM_006716768.3 67 Intron XP_006716831.1
Gene
TMEM8B
Gene Name
transmembrane protein 8B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001042589.2 67 Intron NP_001036054.1
NM_001042590.2 67 Intron NP_001036055.1
NM_016446.3 67 Intron NP_057530.2
XM_005251483.4 67 Intron XP_005251540.3
XM_011517901.2 67 Intron XP_011516203.1
XM_011517902.2 67 Intron XP_011516204.1
XM_011517903.2 67 Intron XP_011516205.1
XM_011517904.2 67 UTR 5 XP_011516206.1
XM_011517905.1 67 Intron XP_011516207.1
XM_011517908.2 67 Intron XP_011516210.1
XM_011517910.2 67 Intron XP_011516212.1
XM_011517911.2 67 Intron XP_011516213.1
XM_011517912.2 67 Intron XP_011516214.1
XM_011517913.2 67 Intron XP_011516215.1
XM_011517914.2 67 Intron XP_011516216.1
XM_011517915.2 67 Intron XP_011516217.1
XM_011517916.2 67 Intron XP_011516218.1
XM_011517918.2 67 Intron XP_011516220.1
XM_017014805.1 67 Intron XP_016870294.1
XM_017014806.1 67 Intron XP_016870295.1
XM_017014807.1 67 Intron XP_016870296.1

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