Mutation

Primary Site >> Liver Cancer

Gene >> CLTC

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269122
Start	59677061:59677061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2669C>T
AA Mutation	p.Pro890Leu(p.P890L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269122
Start	59666502:59666502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1805A>G
AA Mutation	p.Asn602Ser(p.N602S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000269122
Start	59681462:59681462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759911857
CDS Mutation	c.3233A>G
AA Mutation	p.Asn1078Ser(p.N1078S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000269122
Start	59661467:59661467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1192A>G
AA Mutation	p.Ile398Val(p.I398V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000269122
Start	59647570:59647570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.423G>A
AA Mutation	p.Met141Ile(p.M141I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000269122
Start	59680987:59680987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2995G>C
AA Mutation	p.Asp999His(p.D999H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000269122
Start	59683909:59683909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748731820
CDS Mutation	c.4358G>A
AA Mutation	p.Arg1453His(p.R1453H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000269122
Start	59655965:59655965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.907A>G
AA Mutation	p.Ile303Val(p.I303V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269122
Start	59681661:59681661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3264T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000269122
Start	59660401:59660440(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.983_1022delGTGTGGAAGAAGAAAACATAATTCCTTACATCACCAATGT
AA Mutation	p.Cys328PhefsTer9(p.C328Ffs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript