Colon Cancer: Gene >> LRCH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000389798
Start	46699342:46699342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1252G>A
AA Mutation	p.Ala418Thr(p.A418T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000389798
Start	46692613:46692613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1092C>A
AA Mutation	p.Asp364Glu(p.D364E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000389798
Start	46728941:46728941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1859G>A
AA Mutation	p.Arg620His(p.R620H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000389798
Start	46692615:46692615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141234801
CDS Mutation	c.1094C>T
AA Mutation	p.Ser365Leu(p.S365L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000389798
Start	46728939:46728939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1857C>G
AA Mutation	p.Ile619Met(p.I619M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000389798
Start	46705111:46705111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1444C>T
AA Mutation	p.Pro482Ser(p.P482S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000389798
Start	46741756:46741756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267603839
CDS Mutation	c.2095C>T
AA Mutation	p.Arg699Cys(p.R699C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389798
Start	46741818:46741818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2157C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389798
Start	46669090:46669090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.513C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000389798
Start	46553553:46553553(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.161delG
AA Mutation	p.Gly54AlafsTer6(p.G54Afs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> LRCH1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000389798
Start	46669032:46669032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.455G>A
AA Mutation	p.Arg152Gln(p.R152Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000389798
Start	46741834:46741834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2173G>T
AA Mutation	p.Ala725Ser(p.A725S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000389798
Start	46685952:46685952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.733G>A
AA Mutation	p.Val245Met(p.V245M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311191
Start	46750632:46750632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2073G>A
Mutation Classification	Silent
Feature Type	Transcript