HDAC9 c.436G>C ;(p.V146L)

Variant ID: 7-18631159-G-C

NM_178425.2(HDAC9):c.436G>C;(p.V146L)

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:

Whole genome deep sequencing analysis of cell-free DNA in samples with low tumour content.

Bmc Cancer
Ganesamoorthy, Devika D; Robertson, Alan James AJ; Chen, Wenhan W; Hall, Michael B MB; Cao, Minh Duc MD; Ferguson, Kaltin K; Lakhani, Sunil R SR; Nones, Katia K; Simpson, Peter T PT; Coin, Lachlan J M LJM
Publication Date: 2022-01-20

Variant appearance in text: HDAC9: V146L
PubMed Link: 35057759
Variant Present in the following documents:
  • 12885_2021_9160_MOESM1_ESM.xlsx, sheet 8
View BVdb publication page


Whole genome deep sequencing analysis of cell-free DNA in samples with low tumour content.

Bmc Cancer
Ganesamoorthy, Devika D; Robertson, Alan James AJ; Chen, Wenhan W; Hall, Michael B MB; Cao, Minh Duc MD; Ferguson, Kaltin K; Lakhani, Sunil R SR; Nones, Katia K; Simpson, Peter T PT; Coin, Lachlan J M LJM
Publication Date: 2022-01-20

Variant appearance in text: HDAC9: V146L
PubMed Link: 35057759
Variant Present in the following documents:
  • 12885_2021_9160_MOESM1_ESM.xlsx, sheet 8
View BVdb publication page