UGT2B10 c.353T>G ;(p.I118S)

Variant ID: 4-69682090-T-G

NM_001075.4(UGT2B10):c.353T>G;(p.I118S)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson's Disease.

Scientific Reports
Yemni, Eman Al EA; Monies, Dorota D; Alkhairallah, Thamer T; Bohlega, Saeed S; Abouelhoda, Mohamed M; Magrashi, Amna A; Mustafa, Abeer A; AlAbdulaziz, Basma B; Alhamed, Mohamed M; Baz, Batoul B; Goljan, Ewa E; Albar, Renad R; Jabaan, Amjad A; Faquih, Tariq T; Subhani, Shazia S; Ali, Wafa W; Shinwari, Jameela J; Al-Mubarak, Bashayer B; Al-Tassan, Nada N
Publication Date: 2019-03-04

Variant appearance in text: UGT2B10: 353T>G; I118S
PubMed Link: 30833663
Variant Present in the following documents:
  • 41598_2019_40102_MOESM1_ESM.pdf
View BVdb publication page