Product Details

SNP ID
rs7880002
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.X:102745242 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GACAGGGAAAGGCCCTCTTTTGGGG[G/T]CAACTGTGGGGACGGCGCAATGCCA
Phenotype
MIM: 300921
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
BHLHB9 PubMed Links

Gene Details

Gene
BHLHB9
Gene Name
basic helix-loop-helix domain containing, class B, 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001142524.1 Intron NP_001135996.1
NM_001142525.1 Intron NP_001135997.1
NM_001142526.1 Intron NP_001135998.1
NM_001142527.1 Intron NP_001135999.1
NM_001142528.1 Intron NP_001136000.1
NM_001142529.1 Intron NP_001136001.1
NM_001142530.1 Intron NP_001136002.1
NM_030639.2 Intron NP_085142.1

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