Colon Cancer: Gene >> LRRC4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000249363
Start	128030354:128030354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746701145
CDS Mutation	c.287G>A
AA Mutation	p.Arg96His(p.R96H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000249363
Start	128029851:128029851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.790G>T
AA Mutation	p.Gly264Trp(p.G264W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000249363
Start	128029472:128029472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1169C>T
AA Mutation	p.Thr390Ile(p.T390I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000249363
Start	128028984:128028984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1657C>T
AA Mutation	p.Arg553Trp(p.R553W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000249363
Start	128028842:128028842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1799C>T
AA Mutation	p.Thr600Ile(p.T600I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000249363
Start	128029271:128029271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1370T>C
AA Mutation	p.Val457Ala(p.V457A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249363
Start	128029180:128029180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1461T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249363
Start	128029759:128029759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.882G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249363
Start	128029549:128029549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202181902
CDS Mutation	c.1092T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249363
Start	128030251:128030251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764268218
CDS Mutation	c.390G>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LRRC4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000249363
Start	128029425:128029425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778062327
CDS Mutation	c.1216G>A
AA Mutation	p.Asp406Asn(p.D406N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript