Product Details

SNP ID: rs41264495
Assay Type: Functionally tested
NCBI dbSNP Submissions: 12
Location: Chr.1:39624371 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGAAAGAGCTGGATCATTCCCATCT[A/C]ATTTCAGTGGCATCACAGATTCTTT
Phenotype: MIM: 609034
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: HEYL PubMed Links

Gene Details

Gene: HEYL
Gene Name: hes related family bHLH transcription factor with YRPW motif-like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014571.3	3174	UTR 3			NP_055386.1
XM_005270745.2	3174	UTR 3			XP_005270802.1