Colon Cancer: Gene >> TNFAIP6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000243347
Start	151366170:151366170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200351871
CDS Mutation	c.347G>A
AA Mutation	p.Arg116His(p.R116H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000243347
Start	151370037:151370037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564029423
CDS Mutation	c.412G>A
AA Mutation	p.Val138Ile(p.V138I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000243347
Start	151366169:151366169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373227124
CDS Mutation	c.346C>T
AA Mutation	p.Arg116Cys(p.R116C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000243347
Start	151379444:151379444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.745C>A
AA Mutation	p.Pro249Thr(p.P249T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000243347
Start	151370090:151370090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755909985
CDS Mutation	c.465C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000243347
Start	151370231:151370231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.606C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000243347
Start	151379491:151379491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.792T>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TNFAIP6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000243347
Start	151364008:151364008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160G>A
AA Mutation	p.Ala54Thr(p.A54T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000243347
Start	151379472:151379472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.773A>C
AA Mutation	p.Asn258Thr(p.N258T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript