Colon Cancer: Gene >> MTCH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373627
Start	36977215:36977215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.685C>T
AA Mutation	p.Arg229Trp(p.R229W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373627
Start	36978105:36978105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.564G>T
AA Mutation	p.Lys188Asn(p.K188N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373627
Start	36968940:36968940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1133G>A
AA Mutation	p.Arg378His(p.R378H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373627
Start	36970069:36970069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1068G>T
AA Mutation	p.Trp356Cys(p.W356C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373627
Start	36972656:36972656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.902C>T
AA Mutation	p.Ser301Phe(p.S301F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373627
Start	36978577:36978577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140514687
CDS Mutation	c.441G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000373627
Start	36968962:36968962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1111C>T
AA Mutation	p.Arg371Ter(p.R371*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MTCH1

No Mutation Annotation!