Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FGF9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382353
Start	21672021:21672021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.109C>A
AA Mutation	p.Leu37Met(p.L37M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000382353
Start	21701229:21701229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.421G>A
AA Mutation	p.Glu141Lys(p.E141K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000382353
Start	21681086:21681086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.322C>T
AA Mutation	p.Arg108Ter(p.R108*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000382353
Start	21672001:21672002(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.89_90insA
AA Mutation	p.Val31GlyfsTer5(p.V31Gfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000382353
Start	21672003:21672004(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.91_92insAGATA
AA Mutation	p.Val31GlufsTer5(p.V31Efs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FGF9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382353
Start	21671945:21671945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.33C>A
AA Mutation	p.Phe11Leu(p.F11L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382353
Start	21672086:21672086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.174G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000382353
Start	21701232:21701232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.424G>T
AA Mutation	p.Glu142Ter(p.E142*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript