Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FGF8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344255
Start	101770378:101770378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137852664
CDS Mutation	c.653C>T
AA Mutation	p.Thr218Met(p.T218M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344255
Start	101774767:101774767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.269G>A
AA Mutation	p.Arg90His(p.R90H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000344255
Start	101774744:101774744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.292G>A
AA Mutation	p.Gly98Ser(p.G98S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000344255
Start	101770483:101770483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.548C>T
AA Mutation	p.Thr183Met(p.T183M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344255
Start	101774760:101774760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.276C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FGF8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344255
Start	101775180:101775180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.106C>A
AA Mutation	p.Leu36Ile(p.L36I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000344255
Start	101770334:101770334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774950983
CDS Mutation	c.697C>T
AA Mutation	p.Arg233Ter(p.R233*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000344255
Start	101771522:101771522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.352C>T
AA Mutation	p.Arg118Ter(p.R118*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript