Colon Cancer: Gene >> KRT10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269576
Start	40821978:40821978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.608T>C
AA Mutation	p.Ile203Thr(p.I203T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269576
Start	40820548:40820548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.830C>T
AA Mutation	p.Thr277Ile(p.T277I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000269576
Start	40822119:40822119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs58075662
CDS Mutation	c.467G>A
AA Mutation	p.Arg156His(p.R156H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000269576
Start	40821987:40821987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.599A>G
AA Mutation	p.Tyr200Cys(p.Y200C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000269576
Start	40822093:40822093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779748369
CDS Mutation	c.493C>T
AA Mutation	p.Arg165Trp(p.R165W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000269576
Start	40820644:40820644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369473843
CDS Mutation	c.734G>A
AA Mutation	p.Arg245His(p.R245H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000269576
Start	40822005:40822005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373319671
CDS Mutation	c.581G>A
AA Mutation	p.Arg194His(p.R194H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269576
Start	40820097:40820097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536668934
CDS Mutation	c.1107A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269576
Start	40822256:40822256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.330C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000269576
Start	40820156:40820156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1048G>T
AA Mutation	p.Glu350Ter(p.E350*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> KRT10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269576
Start	40820626:40820626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.752A>G
AA Mutation	p.Asp251Gly(p.D251G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269576
Start	40822226:40822226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.360C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269576
Start	40820067:40820067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1137A>C
Mutation Classification	Silent
Feature Type	Transcript