Colon Cancer: Gene >> HGD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000283871
Start	120633193:120633193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1142C>T
AA Mutation	p.Ala381Val(p.A381V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000283871
Start	120674904:120674904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.173G>T
AA Mutation	p.Arg58Ile(p.R58I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000283871
Start	120633161:120633161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1174G>A
AA Mutation	p.Ala392Thr(p.A392T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000283871
Start	120628476:120628476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1242G>T
AA Mutation	p.Lys414Asn(p.K414N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283871
Start	120644336:120644336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.757C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283871
Start	120670484:120670484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.225C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000283871
Start	120644362:120644362(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.731delC
AA Mutation	p.Thr244ArgfsTer36(p.T244Rfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HGD

No Mutation Annotation!