Product Details

SNP ID
rs4862491
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:185019307 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
GCAGTGTGCGCGGCTGGAGAGGCGG[C/T]TTGCACCCAGCTGCTAGAGCCGCGC
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
HELT PubMed Links

Gene Details

Gene
HELT
Gene Name
helt bHLH transcription factor
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001300781.1 79 Intron NP_001287710.1
NM_001300782.1 79 Intron NP_001287711.1
XM_017008186.1 79 UTR 5 XP_016863675.1

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