Colon Cancer: Gene >> SHH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297261
Start	155806427:155806427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.431G>A
AA Mutation	p.Arg144His(p.R144H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297261
Start	155803018:155803018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780618619
CDS Mutation	c.1271C>T
AA Mutation	p.Pro424Leu(p.P424L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000297261
Start	155811996:155811996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.127G>A
AA Mutation	p.Ala43Thr(p.A43T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000297261
Start	155812071:155812071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.52G>A
AA Mutation	p.Val18Ile(p.V18I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000297261
Start	155806516:155806516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.342G>T
AA Mutation	p.Met114Ile(p.M114I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000297261
Start	155803082:155803082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1207G>A
AA Mutation	p.Gly403Ser(p.G403S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297261
Start	155803023:155803023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1266C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SHH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297261
Start	155811905:155811905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.218T>G
AA Mutation	p.Phe73Cys(p.F73C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript