Colon Cancer: Gene >> TNFAIP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000226225
Start	28341407:28341407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782624780
CDS Mutation	c.469G>A
AA Mutation	p.Val157Met(p.V157M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000226225
Start	28342278:28342278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.550G>A
AA Mutation	p.Glu184Lys(p.E184K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000226225
Start	28344463:28344463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782727172
CDS Mutation	c.814C>T
AA Mutation	p.Arg272Cys(p.R272C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000226225
Start	28342315:28342315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782444724
CDS Mutation	c.587G>A
AA Mutation	p.Arg196His(p.R196H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000226225
Start	28341306:28341306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.445C>T
AA Mutation	p.Leu149Phe(p.L149F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000226225
Start	28344441:28344443(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.794_796delCCT
AA Mutation	p.Ser265del(p.S265del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TNFAIP1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226225
Start	28342277:28342277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560731179
CDS Mutation	c.549C>T
Mutation Classification	Silent
Feature Type	Transcript