Colon Cancer: Gene >> FOXL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330315
Start	138946511:138946511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.212C>T
AA Mutation	p.Ala71Val(p.A71V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330315
Start	138946577:138946577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.146C>T
AA Mutation	p.Pro49Leu(p.P49L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000330315
Start	138946521:138946521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.202C>T
AA Mutation	p.Arg68Cys(p.R68C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000330315
Start	138946254:138946254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758370933
CDS Mutation	c.469C>G
AA Mutation	p.Pro157Ala(p.P157A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000330315
Start	138946496:138946496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.227C>T
AA Mutation	p.Thr76Met(p.T76M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000330315
Start	138946290:138946290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.433C>T
AA Mutation	p.Arg145Cys(p.R145C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FOXL2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330315
Start	138945628:138945628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1095C>T
Mutation Classification	Silent
Feature Type	Transcript