Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TXNIP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000582401
Start	145996241:145996241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.26C>A
AA Mutation	p.Ser9Tyr(p.S9Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000582401
Start	145993886:145993886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1141G>A
AA Mutation	p.Val381Met(p.V381M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000582401
Start	145994942:145994942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.561A>C
AA Mutation	p.Lys187Asn(p.K187N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000582401
Start	145995026:145995026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.477T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000582401
Start	145994070:145994070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1086T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000582401
Start	145994092:145994093(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1063_1064delAT
AA Mutation	p.Met355GlyfsTer14(p.M355Gfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TXNIP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000582401
Start	145994096:145994096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1060G>A
AA Mutation	p.Asp354Asn(p.D354N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000582401
Start	145996241:145996241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.26C>A
AA Mutation	p.Ser9Tyr(p.S9Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000582401
Start	145995003:145995005(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.498_500delGAA
AA Mutation	p.Lys167del(p.K167del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript