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CYBB c.1535G>C ;(p.G512A)
Variant ID: X-37668893-G-C
NM_000397.3(
CYBB
):c.1535G>C;(p.G512A)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Cancer neoantigen prioritization through sensitive and reliable proteogenomics analysis.
Nature Communications
Wen, Bo B; Li, Kai K; Zhang, Yun Y; Zhang, Bing B
Publication Date: 2020-04-09
Variant appearance in text: CYBB: G512A
PubMed Link:
32273506
Variant Present in the following documents:
41467_2020_15456_MOESM6_ESM.xlsx, sheet 1
View BVdb publication page
Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases.
Scientific Reports
Šimčíková, Daniela D; Heneberg, Petr P
Publication Date: 2019-12-09
Variant appearance in text: CYBB: G512A
PubMed Link:
31819097
Variant Present in the following documents:
41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page