Colon Cancer: Gene >> C1S

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328916
Start	7065109:7065109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.527G>T
AA Mutation	p.Ser176Ile(p.S176I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328916
Start	7066566:7066566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs78558058
CDS Mutation	c.920C>T
AA Mutation	p.Ala307Val(p.A307V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328916
Start	7070181:7070181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1597G>A
AA Mutation	p.Val533Met(p.V533M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000328916
Start	7070031:7070031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781887755
CDS Mutation	c.1447C>T
AA Mutation	p.Pro483Ser(p.P483S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000328916
Start	7069911:7069911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781845594
CDS Mutation	c.1327G>A
AA Mutation	p.Asp443Asn(p.D443N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000328916
Start	7062549:7062549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.80A>C
AA Mutation	p.Asn27Thr(p.N27T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328916
Start	7062517:7062517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.48G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328916
Start	7065164:7065164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.582A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328916
Start	7064355:7064355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782374131
CDS Mutation	c.480G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328916
Start	7067068:7067068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782535131
CDS Mutation	c.1017G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328916
Start	7070219:7070219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1635C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328916
Start	7070553:7070553(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1972delC
AA Mutation	p.Gln658SerfsTer11(p.Q658Sfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000328916
Start	7062505:7062505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.36G>A
AA Mutation	p.Trp12Ter(p.W12*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328916
Start	7065934:7065935(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.842dupA
AA Mutation	p.Trp283LeufsTer14(p.W283Lfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328916
Start	7064348:7064349(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.479dupC
AA Mutation	p.Glu161GlyfsTer6(p.E161Gfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328916
Start	7070634:7070635(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2056dupC
AA Mutation	p.Arg686ProfsTer2(p.R686Pfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> C1S

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328916
Start	7070152:7070152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1568G>A
AA Mutation	p.Arg523Gln(p.R523Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328916
Start	7067046:7067046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.995T>C
AA Mutation	p.Val332Ala(p.V332A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328916
Start	7066567:7066567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782012840
CDS Mutation	c.921G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328916
Start	7063016:7063016(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.343delT
AA Mutation	p.Ser115ProfsTer18(p.S115Pfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript