Colon Cancer: Gene >> LGSN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370657
Start	63280043:63280043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1508A>C
AA Mutation	p.Lys503Thr(p.K503T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370657
Start	63280401:63280401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1150T>C
AA Mutation	p.Trp384Arg(p.W384R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370657
Start	63285705:63285705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761631352
CDS Mutation	c.212C>T
AA Mutation	p.Ser71Phe(p.S71F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370657
Start	63280271:63280271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1280G>A
AA Mutation	p.Gly427Asp(p.G427D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370657
Start	63280448:63280448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765583125
CDS Mutation	c.1103G>A
AA Mutation	p.Arg368His(p.R368H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370657
Start	63280538:63280538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372668010
CDS Mutation	c.1013C>T
AA Mutation	p.Thr338Met(p.T338M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370657
Start	63280546:63280546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1005G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370657
Start	63280537:63280537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756580891
CDS Mutation	c.1014G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370657
Start	63280522:63280522(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1029delA
AA Mutation	p.Lys343AsnfsTer7(p.K343Nfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000370657
Start	63280680:63280680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.871G>T
AA Mutation	p.Glu291Ter(p.E291*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000370657
Start	63294937:63294937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.139G>T
AA Mutation	p.Glu47Ter(p.E47*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370657
Start	63280545:63280546(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1005_1006insAT
AA Mutation	p.Gln336IlefsTer15(p.Q336Ifs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> LGSN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370657
Start	63295001:63295001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.75G>T
AA Mutation	p.Met25Ile(p.M25I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript