Colon Cancer: Gene >> LAMP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000200639
Start	120469135:120469135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.35C>T
AA Mutation	p.Ser12Leu(p.S12L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000200639
Start	120455378:120455378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.376T>C
AA Mutation	p.Phe126Leu(p.F126L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000200639
Start	120455485:120455485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.269T>C
AA Mutation	p.Val90Ala(p.V90A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000200639
Start	120441742:120441742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1081A>C
AA Mutation	p.Lys361Gln(p.K361Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000200639
Start	120431402:120431402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1154T>C
AA Mutation	p.Leu385Ser(p.L385S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000200639
Start	120469130:120469130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.40C>A
AA Mutation	p.Leu14Ile(p.L14I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000200639
Start	120447907:120447907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.675T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000200639
Start	120431437:120431437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1119C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000200639
Start	120431380:120431380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758020252
CDS Mutation	c.1176G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LAMP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000200639
Start	120447930:120447930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.652C>A
AA Mutation	p.Pro218Thr(p.P218T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000200639
Start	120455454:120455454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765548221
CDS Mutation	c.300G>A
Mutation Classification	Silent
Feature Type	Transcript