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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