Mutation

Primary Site >> Liver Cancer

Gene >> ALK

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000389048
Start	29717666:29717666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.699G>T
AA Mutation	p.Met233Ile(p.M233I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000389048
Start	29920344:29920344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.316C>T
AA Mutation	p.Pro106Ser(p.P106S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000389048
Start	29251109:29251109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2200T>A
AA Mutation	p.Tyr734Asn(p.Y734N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000389048
Start	29228941:29228941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2758G>T
AA Mutation	p.Gly920Cys(p.G920C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000389048
Start	29328410:29328410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1354G>T
AA Mutation	p.Gly452Trp(p.G452W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000389048
Start	29920044:29920044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141093002
CDS Mutation	c.616G>A
AA Mutation	p.Ala206Thr(p.A206T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000389048
Start	29275192:29275192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1948C>A
AA Mutation	p.Pro650Thr(p.P650T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000389048
Start	29193655:29193655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4432A>G
AA Mutation	p.Met1478Val(p.M1478V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389048
Start	29328435:29328435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1329T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000389048
Start	29220746:29220746(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3605delG
AA Mutation	p.Gly1202GlufsTer56(p.G1202Efs*56)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript