Product Details

SNP ID
rs9366135
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.6:170304694 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TGCTTCCTGCTCCCCTCAGCATGAA[C/T]CTCCTGCGCATGAGAGTTTGGTCTC
Phenotype
MIM: 612266
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
FAM120B PubMed Links

Gene Details

Gene
FAM120B
Gene Name
family with sequence similarity 120B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286379.1 Intron NP_001273308.1
NM_001286380.1 Intron NP_001273309.1
NM_001286381.1 Intron NP_001273310.1
NM_032448.2 Intron NP_115824.1
XM_011536185.2 Intron XP_011534487.1
XM_017011357.1 Intron XP_016866846.1
XM_017011358.1 Intron XP_016866847.1
XM_017011359.1 Intron XP_016866848.1
XM_017011360.1 Intron XP_016866849.1

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