Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> GTF2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370500
Start	88853280:88853280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760691499
CDS Mutation	c.884G>A
AA Mutation	p.Arg295Gln(p.R295Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370500
Start	88857476:88857476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769046476
CDS Mutation	c.547G>A
AA Mutation	p.Val183Ile(p.V183I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370500
Start	88860150:88860150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144944840
CDS Mutation	c.395G>A
AA Mutation	p.Arg132Gln(p.R132Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370500
Start	88857445:88857445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.578G>A
AA Mutation	p.Arg193Gln(p.R193Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370500
Start	88864093:88864093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.146G>T
AA Mutation	p.Gly49Val(p.G49V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000370500
Start	88860280:88860280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.265G>T
AA Mutation	p.Gly89Ter(p.G89*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GTF2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370500
Start	88860235:88860235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.310C>T
AA Mutation	p.Arg104Trp(p.R104W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370500
Start	88857228:88857228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.795A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000370500
Start	88860187:88860187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.358G>T
AA Mutation	p.Glu120Ter(p.E120*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript