Colon Cancer: Gene >> TNFRSF10D

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312584
Start	23163905:23163905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.31G>A
AA Mutation	p.Ala11Thr(p.A11T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312584
Start	23144592:23144592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149257537
CDS Mutation	c.812C>T
AA Mutation	p.Ala271Val(p.A271V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000312584
Start	23145863:23145863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.541A>G
AA Mutation	p.Lys181Glu(p.K181E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000312584
Start	23137883:23137883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373138944
CDS Mutation	c.1148C>T
AA Mutation	p.Thr383Met(p.T383M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000312584
Start	23144605:23144605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752982831
CDS Mutation	c.799C>T
AA Mutation	p.Arg267Ter(p.R267*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TNFRSF10D

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312584
Start	23144534:23144534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.870C>A
Mutation Classification	Silent
Feature Type	Transcript