Colon Cancer: Gene >> STIL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360380
Start	47287561:47287561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1123T>C
AA Mutation	p.Ser375Pro(p.S375P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360380
Start	47251243:47251243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3757C>A
AA Mutation	p.Pro1253Thr(p.P1253T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360380
Start	47251810:47251810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3190G>A
AA Mutation	p.Ala1064Thr(p.A1064T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360380
Start	47280759:47280759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1699C>A
AA Mutation	p.Pro567Thr(p.P567T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360380
Start	47272139:47272139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2320G>T
AA Mutation	p.Val774Leu(p.V774L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360380
Start	47280461:47280461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1997G>A
AA Mutation	p.Arg666Lys(p.R666K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360380
Start	47301719:47301719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.295C>T
AA Mutation	p.Arg99Cys(p.R99C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000360380
Start	47302237:47302237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751248289
CDS Mutation	c.262G>A
AA Mutation	p.Glu88Lys(p.E88K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360380
Start	47269733:47269733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2517A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360380
Start	47287610:47287610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1074A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360380
Start	47280910:47280910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1548C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360380
Start	47280757:47280757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368458430
CDS Mutation	c.1701G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360380
Start	47280835:47280835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1623T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360380
Start	47293529:47293529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.801T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360380
Start	47280793:47280793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1665C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000360380
Start	47301620:47301620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.394G>T
AA Mutation	p.Glu132Ter(p.E132*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> STIL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360380
Start	47269828:47269828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2422G>A
AA Mutation	p.Glu808Lys(p.E808K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360380
Start	47302324:47302324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.175G>C
AA Mutation	p.Glu59Gln(p.E59Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360380
Start	47269762:47269762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773975947
CDS Mutation	c.2488G>A
AA Mutation	p.Asp830Asn(p.D830N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360380
Start	47280602:47280602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1856C>A
AA Mutation	p.Ser619Tyr(p.S619Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360380
Start	47295783:47295783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.767C>A
AA Mutation	p.Ser256Tyr(p.S256Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript