Colon Cancer: Gene >> CTGF

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000367976
Start	131949949:131949949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.753G>T
AA Mutation	p.Lys251Asn(p.K251N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367976
Start	131950119:131950119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.583A>G
AA Mutation	p.Ile195Val(p.I195V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367976
Start	131950136:131950136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.566G>A
AA Mutation	p.Gly189Asp(p.G189D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367976
Start	131949274:131949274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1040A>G
AA Mutation	p.Asp347Gly(p.D347G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367976
Start	131949393:131949393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.921C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367976
Start	131949456:131949456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.858A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CTGF

No Mutation Annotation!