Colon Cancer: Gene >> KRT12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000251643
Start	40866192:40866192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.613G>A
AA Mutation	p.Asp205Asn(p.D205N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000251643
Start	40863801:40863801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754381713
CDS Mutation	c.871G>A
AA Mutation	p.Gly291Arg(p.G291R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000251643
Start	40863199:40863199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1240C>T
AA Mutation	p.Arg414Trp(p.R414W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000251643
Start	40863607:40863607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146332400
CDS Mutation	c.973G>A
AA Mutation	p.Gly325Arg(p.G325R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251643
Start	40867118:40867118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.69G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000251643
Start	40867023:40867023(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.164delG
AA Mutation	p.Gly55GlufsTer56(p.G55Efs*56)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000251643
Start	40863802:40863802(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.870delC
AA Mutation	p.Gly291GlufsTer75(p.G291Efs*75)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000251643
Start	40866715:40866715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.472C>T
AA Mutation	p.Arg158Ter(p.R158*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> KRT12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000251643
Start	40863221:40863221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1218G>T
AA Mutation	p.Glu406Asp(p.E406D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript