Colon Cancer: Gene >> INSC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379554
Start	15112477:15112477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200115207
CDS Mutation	c.8G>A
AA Mutation	p.Arg3Gln(p.R3Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379554
Start	15225737:15225737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1220G>A
AA Mutation	p.Cys407Tyr(p.C407Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379554
Start	15221588:15221588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552439006
CDS Mutation	c.1072G>A
AA Mutation	p.Val358Ile(p.V358I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379554
Start	15175950:15175950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776484741
CDS Mutation	c.407G>A
AA Mutation	p.Arg136His(p.R136H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379554
Start	15175808:15175808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201429164
CDS Mutation	c.265G>A
AA Mutation	p.Glu89Lys(p.E89K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000379554
Start	15177161:15177161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.594G>T
AA Mutation	p.Glu198Asp(p.E198D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000379554
Start	15240503:15240503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201482506
CDS Mutation	c.1591G>A
AA Mutation	p.Ala531Thr(p.A531T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000379554
Start	15190717:15190717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.737T>A
AA Mutation	p.Ile246Asn(p.I246N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000379554
Start	15175819:15175819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.276T>G
AA Mutation	p.Cys92Trp(p.C92W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000379554
Start	15200824:15200824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.835G>C
AA Mutation	p.Glu279Gln(p.E279Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379554
Start	15176005:15176005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.462C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379554
Start	15221599:15221599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1083C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379554
Start	15175807:15175807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.264C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000379554
Start	15225661:15225661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1144G>T
AA Mutation	p.Glu382Ter(p.E382*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> INSC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379554
Start	15245921:15245921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199686458
CDS Mutation	c.1621C>T
AA Mutation	p.Arg541Cys(p.R541C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379554
Start	15112527:15112527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.58C>A
AA Mutation	p.Leu20Ile(p.L20I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379554
Start	15225756:15225756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1239G>T
AA Mutation	p.Leu413Phe(p.L413F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379554
Start	15221584:15221584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1068G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000379554
Start	15112566:15112566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368896159
CDS Mutation	c.96+1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript