Colon Cancer: Gene >> KRT23

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000209718
Start	40928284:40928284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115236336
CDS Mutation	c.875G>A
AA Mutation	p.Arg292His(p.R292H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000209718
Start	40925474:40925474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141349810
CDS Mutation	c.1022C>T
AA Mutation	p.Thr341Met(p.T341M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000209718
Start	40936458:40936458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.146C>T
AA Mutation	p.Thr49Met(p.T49M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000209718
Start	40936491:40936491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746484267
CDS Mutation	c.113C>T
AA Mutation	p.Ala38Val(p.A38V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000209718
Start	40936359:40936359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138435929
CDS Mutation	c.245G>A
AA Mutation	p.Arg82His(p.R82H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000209718
Start	40931419:40931419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775234590
CDS Mutation	c.433C>A
AA Mutation	p.Leu145Ile(p.L145I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000209718
Start	40925422:40925422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1074G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000209718
Start	40936534:40936534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.70C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> KRT23

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000209718
Start	40928479:40928479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.765G>A
Mutation Classification	Silent
Feature Type	Transcript