Colon Cancer: Gene >> LAMP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332556
Start	113321580:113321580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371034089
CDS Mutation	c.967G>A
AA Mutation	p.Gly323Ser(p.G323S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000332556
Start	113321646:113321646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767683537
CDS Mutation	c.1033C>T
AA Mutation	p.Arg345Cys(p.R345C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000332556
Start	113310717:113310717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.412A>G
AA Mutation	p.Thr138Ala(p.T138A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000332556
Start	113321659:113321659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757618803
CDS Mutation	c.1046C>T
AA Mutation	p.Ala349Val(p.A349V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000332556
Start	113320346:113320346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370286796
CDS Mutation	c.752C>T
AA Mutation	p.Thr251Met(p.T251M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000332556
Start	113322336:113322336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1169G>A
AA Mutation	p.Gly390Asp(p.G390D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332556
Start	113321609:113321609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374840461
CDS Mutation	c.996C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332556
Start	113321633:113321633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372087869
CDS Mutation	c.1020G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332556
Start	113309651:113309651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.192C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LAMP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332556
Start	113310735:113310735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.430G>T
AA Mutation	p.Asp144Tyr(p.D144Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332556
Start	113320440:113320440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777585404
CDS Mutation	c.846C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332556
Start	113320401:113320401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761301142
CDS Mutation	c.807C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332556
Start	113321654:113321654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376013627
CDS Mutation	c.1041G>A
Mutation Classification	Silent
Feature Type	Transcript