Colon Cancer: Gene >> KCNC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379472
Start	17772400:17772400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1306G>A
AA Mutation	p.Val436Met(p.V436M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379472
Start	17772277:17772277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1183G>A
AA Mutation	p.Val395Met(p.V395M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379472
Start	17736522:17736522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.520C>T
AA Mutation	p.Pro174Ser(p.P174S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379472
Start	17772323:17772323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1229C>T
AA Mutation	p.Thr410Met(p.T410M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379472
Start	17736196:17736196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.194C>T
AA Mutation	p.Ala65Val(p.A65V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000379472
Start	17736183:17736183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.181C>T
AA Mutation	p.Pro61Ser(p.P61S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000379472
Start	17736353:17736353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.351G>T
AA Mutation	p.Glu117Asp(p.E117D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379472
Start	17736371:17736371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.369C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379472
Start	17772531:17772531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1437A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379472
Start	17771793:17771793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.699G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379472
Start	17772318:17772318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779961591
CDS Mutation	c.1224G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379472
Start	17771811:17771811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143670270
CDS Mutation	c.717C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379472
Start	17736140:17736140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.138C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379472
Start	17772457:17772457(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1370delA
AA Mutation	p.Lys457ArgfsTer20(p.K457Rfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379472
Start	17772456:17772457(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1370dupA
AA Mutation	p.Lys458GlufsTer16(p.K458Efs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KCNC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379472
Start	17736243:17736243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.241G>A
AA Mutation	p.Asp81Asn(p.D81N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379472
Start	17772617:17772617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1523G>A
AA Mutation	p.Gly508Asp(p.G508D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379472
Start	17736251:17736251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.249C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379472
Start	17736254:17736254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757220535
CDS Mutation	c.252G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379472
Start	17772411:17772411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776064757
CDS Mutation	c.1317C>T
Mutation Classification	Silent
Feature Type	Transcript