Home
Downloads
UCSC Genome Browser Track
Email Updates
Menu
Varaico: Literature-Extracted Genetic Variants
hg38
Include likely false extractions
Gene:
APRT
Variant:
p.W98delFs
Back to variants list
APRT
NM_000485.3:p.W98delFs
hg38:chr16:88810450 CCA>C
Frequencies & domains
Associated Papers
Gene panel sequencing identifies a likely monogenic cause in 7% of 235 Pakistani families with nephrolithiasis.
Amar A et al.
Human Genetics,
2019
30778725 (PubMed
)
Select a paper to view details