Colon Cancer: Gene >> KRT24

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264651
Start	40701211:40701211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.784C>T
AA Mutation	p.Arg262Cys(p.R262C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264651
Start	40699656:40699656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1149C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264651
Start	40703583:40703583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.111C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264651
Start	40698614:40698614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1398A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264651
Start	40698318:40698318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1497T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264651
Start	40700282:40700282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776478694
CDS Mutation	c.957G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264651
Start	40703529:40703529(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.165delG
AA Mutation	p.Ser56LeufsTer18(p.S56Lfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> KRT24

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264651
Start	40700225:40700225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1014G>T
AA Mutation	p.Lys338Asn(p.K338N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264651
Start	40701197:40701197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.798G>T
AA Mutation	p.Glu266Asp(p.E266D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264651
Start	40703291:40703291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200550767
CDS Mutation	c.403C>A
AA Mutation	p.Leu135Ile(p.L135I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264651
Start	40703290:40703290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.404T>C
AA Mutation	p.Leu135Pro(p.L135P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264651
Start	40699617:40699617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1188C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264651
Start	40699530:40699530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139679856
CDS Mutation	c.1275C>T
Mutation Classification	Silent
Feature Type	Transcript