Colon Cancer: Gene >> VTN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000226218
Start	28368890:28368890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781794064
CDS Mutation	c.808C>T
AA Mutation	p.Arg270Trp(p.R270W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000226218
Start	28367918:28367918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781811496
CDS Mutation	c.1121G>A
AA Mutation	p.Arg374His(p.R374H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000226218
Start	28367874:28367874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1165C>A
AA Mutation	p.Arg389Ser(p.R389S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000226218
Start	28368976:28368976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781794013
CDS Mutation	c.722G>A
AA Mutation	p.Arg241Gln(p.R241Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000226218
Start	28367457:28367457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782315239
CDS Mutation	c.1349G>A
AA Mutation	p.Arg450His(p.R450H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000226218
Start	28369368:28369368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782250181
CDS Mutation	c.590G>A
AA Mutation	p.Arg197Gln(p.R197Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000226218
Start	28368952:28368952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.746G>A
AA Mutation	p.Gly249Asp(p.G249D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000226218
Start	28368956:28368956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782244379
CDS Mutation	c.742G>A
AA Mutation	p.Asp248Asn(p.D248N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000226218
Start	28367954:28367954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568589200
CDS Mutation	c.1085G>A
AA Mutation	p.Arg362His(p.R362H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000226218
Start	28367458:28367458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781937745
CDS Mutation	c.1348C>T
AA Mutation	p.Arg450Cys(p.R450C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226218
Start	28368966:28368966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782011470
CDS Mutation	c.732T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226218
Start	28368019:28368019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374231917
CDS Mutation	c.1020C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226218
Start	28369553:28369553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782463783
CDS Mutation	c.483C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226218
Start	28369652:28369652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.384C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226218
Start	28369664:28369664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375615794
CDS Mutation	c.372G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000226218
Start	28369748:28369748(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.288delC
AA Mutation	p.Ser97ProfsTer2(p.S97Pfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> VTN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000226218
Start	28367419:28367419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201545006
CDS Mutation	c.1387C>T
AA Mutation	p.Arg463Cys(p.R463C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000226218
Start	28369509:28369509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782023049
CDS Mutation	c.527G>A
AA Mutation	p.Arg176Gln(p.R176Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000226218
Start	28368919:28368919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.779T>G
AA Mutation	p.Leu260Arg(p.L260R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000226218
Start	28369552:28369552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782542357
CDS Mutation	c.484G>A
AA Mutation	p.Asp162Asn(p.D162N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000226218
Start	28369532:28369532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.504G>T
AA Mutation	p.Lys168Asn(p.K168N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226218
Start	28368939:28368939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782405279
CDS Mutation	c.759C>T
Mutation Classification	Silent
Feature Type	Transcript