Colon Cancer: Gene >> INVS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262457
Start	100240225:100240225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.781T>C
AA Mutation	p.Trp261Arg(p.W261R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262457
Start	100226072:100226072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372088206
CDS Mutation	c.284G>A
AA Mutation	p.Arg95His(p.R95H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262457
Start	100292763:100292763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2506A>G
AA Mutation	p.Thr836Ala(p.T836A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262457
Start	100226156:100226156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757534991
CDS Mutation	c.368G>A
AA Mutation	p.Arg123Gln(p.R123Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262457
Start	100292593:100292593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771128055
CDS Mutation	c.2336G>A
AA Mutation	p.Arg779Gln(p.R779Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262457
Start	100292637:100292637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556807161
CDS Mutation	c.2380C>T
AA Mutation	p.Arg794Cys(p.R794C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262457
Start	100104550:100104550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.29C>T
AA Mutation	p.Ala10Val(p.A10V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262457
Start	100292425:100292425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2168A>G
AA Mutation	p.Glu723Gly(p.E723G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262457
Start	100229821:100229821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.609C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262457
Start	100272930:100272930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758665047
CDS Mutation	c.1638C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262457
Start	100242631:100242631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.858C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262457
Start	100297035:100297035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2905C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262457
Start	100284494:100284494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1959T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262457
Start	100292942:100292942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371932940
CDS Mutation	c.2685C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262457
Start	100292701:100292701(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs758373067
CDS Mutation	c.2449delG
AA Mutation	p.Glu817ArgfsTer19(p.E817Rfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000262457
Start	100240210:100240210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.766C>T
AA Mutation	p.Arg256Ter(p.R256*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262457
Start	100300652:100300653(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs760013326
CDS Mutation	c.3182dupA
AA Mutation	p.Asn1061LysfsTer20(p.N1061Kfs*20)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000262457
Start	100297935:100297935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3017-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> INVS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262457
Start	100252304:100252304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1100C>A
AA Mutation	p.Ser367Tyr(p.S367Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262457
Start	100292685:100292685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2428C>T
AA Mutation	p.Arg810Cys(p.R810C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript