Product Details

SNP ID
rs10867367
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.9:69334417 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TATGCTGGTCTGATGCTGCAGAATG[A/T]TTACTCTCAGCTAGTGAGAATGGAG
Phenotype
MIM: 607710
Polymorphism
A/T, Transversion Substitution
Allele Nomenclature
Literature Links
FAM189A2 PubMed Links

Gene Details

Gene
FAM189A2
Gene Name
family with sequence similarity 189 member A2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001127608.1 Intron NP_001121080.1
NM_004816.3 Intron NP_004807.3
XM_005252307.4 Intron XP_005252364.1
XM_017015324.1 Intron XP_016870813.1
XM_017015325.1 Intron XP_016870814.1

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