Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TBX21

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000177694
Start	47744860:47744860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1102C>A
AA Mutation	p.Arg368Ser(p.R368S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000177694
Start	47733867:47733867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.413G>T
AA Mutation	p.Arg138Met(p.R138M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000177694
Start	47744828:47744828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1070C>A
AA Mutation	p.Pro357His(p.P357H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000177694
Start	47733793:47733793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.339G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000177694
Start	47744254:47744254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.828C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000177694
Start	47742661:47742661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.543C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TBX21

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000177694
Start	47744532:47744532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.978G>T
AA Mutation	p.Glu326Asp(p.E326D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000177694
Start	47744959:47744959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1201G>T
AA Mutation	p.Ala401Ser(p.A401S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000177694
Start	47745261:47745261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1503C>T
Mutation Classification	Silent
Feature Type	Transcript