Product Details

SNP ID
rs3793660
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:69327176 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTTCATGTTGAATGAACTTATTGG[A/G]GTACGTGCTGGACTGTGGTGAGTGA
Phenotype
MIM: 607710
Polymorphism
A/G, Transition 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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