Product Details

SNP ID
rs138768651
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:67076289 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGAGTTTTGTCACAGACTTAAAAG[C/T]ACATAGCTACGTGGCAAAACTTTTT
Phenotype
MIM: 606699
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
HELZ PubMed Links

Gene Details

Gene
HELZ
Gene Name
helicase with zinc finger
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_014877.3 7979 UTR 3 NP_055692.2
XM_005257888.4 7979 UTR 3 XP_005257945.1
XM_005257889.4 7979 UTR 3 XP_005257946.1
XM_006722214.3 7979 UTR 3 XP_006722277.1
XM_006722215.3 7979 UTR 3 XP_006722278.1
XM_006722216.3 7979 UTR 3 XP_006722279.1
XM_011525544.2 7979 UTR 3 XP_011523846.1
XM_017025477.1 7979 UTR 3 XP_016880966.1
XM_017025478.1 7979 UTR 3 XP_016880967.1

View Full Product Details