Colon Cancer: Gene >> LETMD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262055
Start	51056165:51056165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.682G>T
AA Mutation	p.Ala228Ser(p.A228S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262055
Start	51049069:51049069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.158T>C
AA Mutation	p.Val53Ala(p.V53A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262055
Start	51058078:51058078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.962G>A
AA Mutation	p.Arg321Lys(p.R321K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> LETMD1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262055
Start	51049036:51049036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.125C>A
AA Mutation	p.Ser42Tyr(p.S42Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262055
Start	51053790:51053790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.403G>A
AA Mutation	p.Val135Ile(p.V135I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262055
Start	51049058:51049058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.147A>G
Mutation Classification	Silent
Feature Type	Transcript