Colon Cancer: Gene >> TNFRSF10A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000221132
Start	23212182:23212182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.337C>T
AA Mutation	p.Leu113Phe(p.L113F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000221132
Start	23200505:23200505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.799G>T
AA Mutation	p.Gly267Cys(p.G267C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000221132
Start	23201857:23201857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.580A>G
AA Mutation	p.Thr194Ala(p.T194A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000221132
Start	23199311:23199311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.969G>T
AA Mutation	p.Leu323Phe(p.L323F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000221132
Start	23200745:23200745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.645G>T
AA Mutation	p.Met215Ile(p.M215I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000221132
Start	23200537:23200537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.767C>T
AA Mutation	p.Ala256Val(p.A256V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000221132
Start	23199346:23199347(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.933_934delTG
AA Mutation	p.Glu312AlafsTer32(p.E312Afs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000221132
Start	23197189:23197189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1030G>T
AA Mutation	p.Glu344Ter(p.E344*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TNFRSF10A

No Mutation Annotation!