Mutation

Primary Site >> Liver Cancer

Gene >> MUC6

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1015776:1015776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779736305
CDS Mutation	c.7025C>T
AA Mutation	p.Thr2342Met(p.T2342M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1024067:1024067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752942783
CDS Mutation	c.3262G>A
AA Mutation	p.Asp1088Asn(p.D1088N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1026952:1026952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763956171
CDS Mutation	c.2383G>A
AA Mutation	p.Gly795Ser(p.G795S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1030299:1030299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.929A>T
AA Mutation	p.Glu310Val(p.E310V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1017715:1017715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5086T>A
AA Mutation	p.Ser1696Thr(p.S1696T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000421673
Start	1031883:1031883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756600864
CDS Mutation	c.286C>T
AA Mutation	p.Arg96Trp(p.R96W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421673
Start	1016213:1016213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6588T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421673
Start	1017614:1017614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5187C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421673
Start	1013919:1013919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7122C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000421673
Start	1031239:1031239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.504C>G
AA Mutation	p.Tyr168Ter(p.Y168*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript