Liver Cancer Cell Lines
Database

LCCL to predict drug response

Mutations and CNAs (31)

Gene nameFilter by Gene name	Alteration type	Variant class	Annotation transcript	gNomen	cNomen	pNomen	PPH prédiction	Cell LineFilter by Cell Line
TP53	Mutation	In-Frame	ENST00000269305.4	g.7578269_7578280del g.7578269_7578280del	c.569_580del c.569_580del	p.Pro190_His193del p.Pro190_His193del	damaging damaging	JHH5
TP53	Mutation	Missense	ENST00000269305.4	g.7578475G>A g.7578475G>A	c.455C>T c.455C>T	p.Pro152Leu p.Pro152Leu	probably damaging probably damaging	B1
TP53	Mutation	Missense	ENST00000269305.4	g.7577548C>T g.7577548C>T	c.733G>A c.733G>A	p.Gly245Ser p.Gly245Ser	probably damaging probably damaging	HCC.1.2
TP53	Mutation	Missense	ENST00000269305.4	g.7578205C>A g.7578205C>A	c.644G>T c.644G>T	p.Ser215Ile p.Ser215Ile	probably damaging probably damaging	SNU182
TP53	Mutation	Missense	ENST00000269305.4	g.7578449C>T g.7578449C>T	c.481G>A c.481G>A	p.Ala161Thr p.Ala161Thr	probably damaging probably damaging	SNU449
TP53	Mutation	Missense	ENST00000269305.4	g.7577153C>T g.7577153C>T	c.785G>A c.785G>A	p.Gly262Asp (Splice) p.Gly262Asp (Splice)	probably damaging probably damaging	SNU475
TP53	Mutation	Missense	ENST00000269305.4	g.7577566T>C g.7577566T>C	c.715A>G c.715A>G	p.Asn239Asp p.Asn239Asp	probably damaging probably damaging	SNU475
TP53	Mutation	Missense	ENST00000269305.4	g.7578190T>C g.7578190T>C	c.659A>G c.659A>G	p.Tyr220Cys p.Tyr220Cys	probably damaging probably damaging	Huh7
TP53	Mutation	Missense	ENST00000269305.4	g.7577534C>A g.7577534C>A	c.747G>T c.747G>T	p.Arg249Ser p.Arg249Ser	probably damaging probably damaging	Mahlavu
TP53	Mutation	Missense	ENST00000269305.4	g.7577534C>A g.7577534C>A	c.747G>T c.747G>T	p.Arg249Ser p.Arg249Ser	probably damaging probably damaging	PLC.PRF5
TP53	Mutation	Missense	ENST00000269305.4	g.7577550C>G g.7577550C>G	c.731G>C c.731G>C	p.Gly244Ala p.Gly244Ala	probably damaging probably damaging	HLE
TP53	Mutation	Missense	ENST00000269305.4	g.7577550C>G g.7577550C>G	c.731G>C c.731G>C	p.Gly244Ala p.Gly244Ala	probably damaging probably damaging	HLF
TP53	Mutation	Missense	ENST00000455263.2	g.7576542A>G g.7576542A>G	c.1036T>C c.1036T>C	p.Ser346Pro p.Ser346Pro	benign benign	Li7
TP53	Mutation	Missense	ENST00000455263.2	g.7576572A>C g.7576572A>C	c.1006T>G c.1006T>G	p.Leu336Val p.Leu336Val	damaging damaging	Li7
TP53	Mutation	Missense	ENST00000269305.4	g.7579358C>A g.7579358C>A	c.329G>T c.329G>T	p.Arg110Leu p.Arg110Leu	benign benign	Huh1
TP53	Mutation	Missense	ENST00000269305.4	g.7577534C>A g.7577534C>A	c.747G>T c.747G>T	p.Arg249Ser p.Arg249Ser	probably damaging probably damaging	JHH4
TP53	Mutation	Missense	ENST00000269305.4	g.7577138C>G g.7577138C>G	c.800G>C c.800G>C	p.Arg267Pro p.Arg267Pro	probably damaging probably damaging	JHH7
TP53	Mutation	Missense	ENST00000269305.4	g.7579369G>C g.7579369G>C	c.318C>G c.318C>G	p.Ser106Arg p.Ser106Arg	benign benign	SNU368
TP53	Mutation	Missense	ENST00000269305.4	g.7578204A>C g.7578204A>C	c.645T>G c.645T>G	p.Ser215Arg p.Ser215Arg	probably damaging probably damaging	SNU739
TP53	Mutation	Missense	ENST00000269305.4	g.7577529A>T g.7577529A>T	c.752T>A c.752T>A	p.Ile251Asn p.Ile251Asn	probably damaging probably damaging	SNU878
TP53	Mutation	Truncating	ENST00000269305.4	g.7578475dup g.7578475dup	c.455dup c.455dup	p.Pro153AlafsX28 p.Pro153AlafsX28	damaging damaging	HCC.3
TP53	Mutation	Truncating	ENST00000269305.4	g.7578177C>G g.7578177C>G	c.672G>C c.672G>C	p.Glu224Asp (Splice) p.Glu224Asp (Splice)	damaging damaging	HCC.1.1
TP53	Mutation	Truncating	ENST00000269305.4	g.7578440T>A g.7578440T>A	c.490A>T c.490A>T	p.Lys164X p.Lys164X	damaging damaging	SNU387
TP53	Mutation	Truncating	ENST00000269305.4	g.7578177C>T g.7578177C>T	c.672G>A c.672G>A	p.E224E (Splice) p.E224E (Splice)	damaging damaging	SNU398
TP53	Mutation	Truncating	ENST00000269305.4	g.7578556T>C g.7578556T>C	c.376-2A>G c.376-2A>G	p.Y126_splice p.Y126_splice	damaging damaging	SNU423

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Liver Cancer Cell Lines Database

Molecular Features

Liver Cancer Cell Lines
Database