Colon Cancer: Gene >> EDA2R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374719
Start	66605085:66605085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.229G>A
AA Mutation	p.Ala77Thr(p.A77T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374719
Start	66605193:66605193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.121T>C
AA Mutation	p.Cys41Arg(p.C41R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374719
Start	66605134:66605134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.180T>G
AA Mutation	p.Ser60Arg(p.S60R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374719
Start	66599661:66599661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761044790
CDS Mutation	c.717C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374719
Start	66599551:66599551(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.827delG
AA Mutation	p.Gly276GlufsTer55(p.G276Efs*55)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374719
Start	66599557:66599557(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.821delT
AA Mutation	p.Leu274TrpfsTer57(p.L274Wfs*57)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> EDA2R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374719
Start	66599669:66599669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.709G>A
AA Mutation	p.Ala237Thr(p.A237T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript