Colon Cancer: Gene >> NOTUM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000409678
Start	81956725:81956725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.913C>T
AA Mutation	p.Arg305Cys(p.R305C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000409678
Start	81960746:81960746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.164A>G
AA Mutation	p.Asp55Gly(p.D55G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000409678
Start	81956947:81956947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.823C>T
AA Mutation	p.Arg275Cys(p.R275C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000409678
Start	81956665:81956665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.973T>C
AA Mutation	p.Tyr325His(p.Y325H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000409678
Start	81953043:81953043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1409T>C
AA Mutation	p.Met470Thr(p.M470T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000409678
Start	81954260:81954260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772006556
CDS Mutation	c.1180C>T
AA Mutation	p.Arg394Trp(p.R394W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409678
Start	81955534:81955534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755956448
CDS Mutation	c.999C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409678
Start	81959547:81959547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.396C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409678
Start	81953234:81953234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1218G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NOTUM

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000409678
Start	81953240:81953240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1212G>A
Mutation Classification	Silent
Feature Type	Transcript