Colon Cancer: Gene >> WNT10A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258411
Start	218882241:218882241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.194C>G
AA Mutation	p.Pro65Arg(p.P65R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258411
Start	218881068:218881068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.73C>T
AA Mutation	p.Leu25Phe(p.L25F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000258411
Start	218890028:218890028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779978162
CDS Mutation	c.421G>A
AA Mutation	p.Val141Met(p.V141M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000258411
Start	218892792:218892792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.775C>T
AA Mutation	p.Arg259Trp(p.R259W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000258411
Start	218890206:218890206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.599C>T
AA Mutation	p.Thr200Ile(p.T200I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258411
Start	218882320:218882320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.273C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000258411
Start	218882266:218882267(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.227_228dupTG
AA Mutation	p.Arg77CysfsTer79(p.R77Cfs*79)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> WNT10A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258411
Start	218882255:218882255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146460077
CDS Mutation	c.208C>T
AA Mutation	p.Arg70Trp(p.R70W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript