Colon Cancer: Gene >> LRRC3B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396641
Start	26709845:26709845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.173T>C
AA Mutation	p.Ile58Thr(p.I58T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396641
Start	26709886:26709886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.214G>A
AA Mutation	p.Asp72Asn(p.D72N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000396641
Start	26710022:26710022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.350C>A
AA Mutation	p.Thr117Asn(p.T117N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396641
Start	26710194:26710194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs181467821
CDS Mutation	c.522G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396641
Start	26709981:26709981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.309C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396641
Start	26709687:26709687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.15C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396641
Start	26710267:26710267(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.601delA
AA Mutation	p.Thr201LeufsTer17(p.T201Lfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> LRRC3B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396641
Start	26710279:26710279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.607G>T
AA Mutation	p.Asp203Tyr(p.D203Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396641
Start	26710185:26710185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.513C>A
Mutation Classification	Silent
Feature Type	Transcript