Colon Cancer: Gene >> C9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263408
Start	39315945:39315945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.700A>C
AA Mutation	p.Asn234His(p.N234H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263408
Start	39311317:39311317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371134723
CDS Mutation	c.931C>T
AA Mutation	p.Arg311Cys(p.R311C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263408
Start	39315788:39315788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.857A>G
AA Mutation	p.Tyr286Cys(p.Y286C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263408
Start	39341579:39341579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.305G>A
AA Mutation	p.Gly102Glu(p.G102E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263408
Start	39288780:39288780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1588T>C
AA Mutation	p.Cys530Arg(p.C530R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263408
Start	39288931:39288931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756670408
CDS Mutation	c.1437G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263408
Start	39315820:39315820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.825C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263408
Start	39306689:39306689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1344C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263408
Start	39288769:39288769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1599A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263408
Start	39315994:39315994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141625765
CDS Mutation	c.651C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263408
Start	39315815:39315815(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.830delA
AA Mutation	p.Asn277MetfsTer21(p.N277Mfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263408
Start	39341199:39341199(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.423delC
AA Mutation	p.Cys142AlafsTer6(p.C142Afs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263408
Start	39311371:39311371(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs777158966
CDS Mutation	c.877delA
AA Mutation	p.Met293CysfsTer5(p.M293Cfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263408
Start	39311231:39311232(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1016dupT
AA Mutation	p.Leu339PhefsTer10(p.L339Ffs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> C9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263408
Start	39311372:39311372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.876A>C
AA Mutation	p.Lys292Asn(p.K292N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000263408
Start	39331812:39331812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.479T>C
AA Mutation	p.Ile160Thr(p.I160T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263408
Start	39288793:39288793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1575G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263408
Start	39316021:39316021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139000312
CDS Mutation	c.624C>T
Mutation Classification	Silent
Feature Type	Transcript