Mutation

Primary Site >> Liver Cancer

Gene >> SLC9C1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305815
Start	112179647:112179647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2803A>G
AA Mutation	p.Lys935Glu(p.K935E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000305815
Start	112274900:112274900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.610T>A
AA Mutation	p.Leu204Ile(p.L204I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000305815
Start	112182165:112182165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2617G>T
AA Mutation	p.Asp873Tyr(p.D873Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000305815
Start	112180634:112180634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2678G>T
AA Mutation	p.Cys893Phe(p.C893F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000305815
Start	112277841:112277841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.338C>T
AA Mutation	p.Pro113Leu(p.P113L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000305815
Start	112221207:112221207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1591T>C
AA Mutation	p.Tyr531His(p.Y531H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000305815
Start	112263037:112263037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747653983
CDS Mutation	c.1084C>T
AA Mutation	p.Arg362Cys(p.R362C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000305815
Start	112204229:112204229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201512353
CDS Mutation	c.2161C>T
AA Mutation	p.Arg721Cys(p.R721C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000305815
Start	112244021:112244021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1253T>G
AA Mutation	p.Ile418Ser(p.I418S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305815
Start	112169206:112169206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3042A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000305815
Start	112221138:112221138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1660A>T
AA Mutation	p.Lys554Ter(p.K554*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript