Product Details

SNP ID
rs2390606
Assay Type
Functionally tested
NCBI dbSNP Submissions
42
Location
Chr.1:90712090 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CACCAGTCACACTGCTGTGGGGGAG[A/C]TTTCCAGCCCTGTTTCTAGGGGTGG
Phenotype
MIM: 605212
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
BARHL2 PubMed Links

Gene Details

Gene
BARHL2
Gene Name
BarH like homeobox 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_020063.1 1428 UTR 3 NP_064447.1

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