Colon Cancer: Gene >> LXN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264265
Start	158672378:158672378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758088046
CDS Mutation	c.101T>C
AA Mutation	p.Val34Ala(p.V34A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264265
Start	158666720:158666720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.595G>C
AA Mutation	p.Val199Leu(p.V199L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264265
Start	158670960:158670960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.189A>C
AA Mutation	p.Gln63His(p.Q63H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264265
Start	158672425:158672425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.54G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LXN

No Mutation Annotation!