Colon Cancer: Gene >> FHL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322142
Start	105363360:105363360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.613G>T
AA Mutation	p.Asp205Tyr(p.D205Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322142
Start	105386507:105386507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536715218
CDS Mutation	c.10C>T
AA Mutation	p.Arg4Cys(p.R4C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322142
Start	105373683:105373683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138189036
CDS Mutation	c.207G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FHL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322142
Start	105361398:105361398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs188279857
CDS Mutation	c.725G>A
AA Mutation	p.Arg242Gln(p.R242Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript