Colon Cancer: Gene >> LAPTM4B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000445593
Start	97816062:97816062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.563G>A
AA Mutation	p.Arg188His(p.R188H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000445593
Start	97851411:97851411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147233429
CDS Mutation	c.891G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000445593
Start	97825123:97825123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.846C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000445593
Start	97815347:97815347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.504G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LAPTM4B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000445593
Start	97815354:97815354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.511C>G
AA Mutation	p.Leu171Val(p.L171V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000445593
Start	97851453:97851453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754566573
CDS Mutation	c.933G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000445593
Start	97851459:97851459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.939T>G
Mutation Classification	Silent
Feature Type	Transcript