Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MRGPRX4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314254
Start	18174095:18174095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.839A>G
AA Mutation	p.Gln280Arg(p.Q280R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000314254
Start	18173647:18173647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.391C>T
AA Mutation	p.Arg131Cys(p.R131C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000314254
Start	18173420:18173420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.164G>A
AA Mutation	p.Arg55His(p.R55H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000314254
Start	18173810:18173810(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.560delT
AA Mutation	p.Leu187TyrfsTer25(p.L187Yfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MRGPRX4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314254
Start	18173962:18173962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.706G>A
AA Mutation	p.Gly236Arg(p.G236R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000314254
Start	18173555:18173555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.299C>A
AA Mutation	p.Ser100Tyr(p.S100Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314254
Start	18173394:18173394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.138G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314254
Start	18173598:18173598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774403101
CDS Mutation	c.342C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000314254
Start	18173810:18173810(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.560delT
AA Mutation	p.Leu187TyrfsTer25(p.L187Yfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript