Colon Cancer: Gene >> CNKSR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374253
Start	26183403:26183403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374260381
CDS Mutation	c.742G>A
AA Mutation	p.Glu248Lys(p.E248K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000374253
Start	26180716:26180716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.212G>A
AA Mutation	p.Ser71Asn(p.S71N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374253
Start	26188870:26188870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761159609
CDS Mutation	c.1810C>T
AA Mutation	p.Arg604Trp(p.R604W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374253
Start	26187236:26187236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1398G>T
AA Mutation	p.Lys466Asn(p.K466N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374253
Start	26180531:26180531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.131A>C
AA Mutation	p.Gln44Pro(p.Q44P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374253
Start	26183418:26183418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.757C>A
AA Mutation	p.Arg253Ser(p.R253S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374253
Start	26187447:26187447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1440C>A
AA Mutation	p.Phe480Leu(p.F480L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000374253
Start	26188665:26188665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148602031
CDS Mutation	c.1679G>A
AA Mutation	p.Arg560His(p.R560H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000374253
Start	26187463:26187463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1456A>G
AA Mutation	p.Thr486Ala(p.T486A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374253
Start	26188287:26188287(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs757494428
CDS Mutation	c.1535delC
AA Mutation	p.Pro512HisfsTer58(p.P512Hfs*58)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374253
Start	26189460:26189460(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2080delC
AA Mutation	p.His694ThrfsTer16(p.H694Tfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000374253
Start	26183361:26183361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200619424
CDS Mutation	c.700C>T
AA Mutation	p.Arg234Ter(p.R234*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374253
Start	26188286:26188287(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs753922055
CDS Mutation	c.1535dupC
AA Mutation	p.Pro513ThrfsTer9(p.P513Tfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000374253
Start	26180612:26180612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.210+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CNKSR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374253
Start	26180735:26180735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.231G>T
AA Mutation	p.Glu77Asp(p.E77D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript