Colon Cancer: Gene >> TNFAIP8L2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368910
Start	151158855:151158855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139852088
CDS Mutation	c.158G>A
AA Mutation	p.Arg53Gln(p.R53Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368910
Start	151158920:151158920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759686603
CDS Mutation	c.223C>T
AA Mutation	p.Arg75Cys(p.R75C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368910
Start	151159167:151159167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771999459
CDS Mutation	c.470C>T
AA Mutation	p.Thr157Met(p.T157M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368910
Start	151158843:151158843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.146A>G
AA Mutation	p.Tyr49Cys(p.Y49C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368910
Start	151158762:151158762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777732715
CDS Mutation	c.65C>T
AA Mutation	p.Ala22Val(p.A22V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368910
Start	151158997:151158997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.300G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TNFAIP8L2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368910
Start	151158827:151158827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.130C>T
AA Mutation	p.Arg44Cys(p.R44C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript