SLC2A9 c.38G>A ;(p.G13D)

Variant ID: 4-10023016-C-T

NM_020041.2(SLC2A9):c.38G>A;(p.G13D)

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:

Amplicon targeted resequencing for SLC2A9 and SLC22A12 identified novel mutations in hypouricemia subjects.

Molecular Genetics & Genomic Medicine
Zhou, Zhaowei Z; Wang, Ke K; Zhou, Juan J; Wang, Can C; Li, Xinde X; Cui, Lingling L; Han, Lin L; Liu, Zhen Z; Ren, Wei W; Wang, Xuefeng X; Zhang, Keke K; Li, Zhiqiang Z; Pan, Dun D; Li, Changgui C; Shi, Yongyong Y
Publication Date: 2019-07

Variant appearance in text: SLC2A9: G13D
PubMed Link: 31131560
Variant Present in the following documents:
  • Main text
  • MGG3-7-e00722-s002.xlsx, sheet 3
  • MGG3-7-e00722-s002.xlsx, sheet 2
  • MGG3-7-e00722.pdf
View BVdb publication page