Colon Cancer: Gene >> VNN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367928
Start	132693281:132693281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.569T>C
AA Mutation	p.Val190Ala(p.V190A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367928
Start	132683159:132683159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1523T>C
AA Mutation	p.Val508Ala(p.V508A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367928
Start	132684422:132684422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1272G>T
AA Mutation	p.Met424Ile(p.M424I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367928
Start	132713941:132713941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.95A>G
AA Mutation	p.His32Arg(p.H32R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367928
Start	132684460:132684460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370748066
CDS Mutation	c.1234G>A
AA Mutation	p.Gly412Ser(p.G412S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367928
Start	132692521:132692521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.890G>T
AA Mutation	p.Gly297Val(p.G297V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367928
Start	132693300:132693300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.550G>T
AA Mutation	p.Gly184Cys(p.G184C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367928
Start	132683306:132683306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745392481
CDS Mutation	c.1376G>A
AA Mutation	p.Arg459His(p.R459H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000367928
Start	132693165:132693165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369042237
CDS Mutation	c.685G>A
AA Mutation	p.Val229Met(p.V229M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367928
Start	132692277:132692277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370496023
CDS Mutation	c.1134C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367928
Start	132711714:132711714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148444875
CDS Mutation	c.336T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367928
Start	132683155:132683155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1527C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367928
Start	132713847:132713847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560182070
CDS Mutation	c.189G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367928
Start	132694063:132694063(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.461delC
AA Mutation	p.Pro154LeufsTer44(p.P154Lfs*44)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> VNN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367928
Start	132693059:132693059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.791C>A
AA Mutation	p.Ala264Glu(p.A264E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367928
Start	132693140:132693140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.710C>A
AA Mutation	p.Ala237Asp(p.A237D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367928
Start	132694152:132694152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.372C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367928
Start	132683311:132683311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750178052
CDS Mutation	c.1371C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367928
Start	132683209:132683209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1473C>T
Mutation Classification	Silent
Feature Type	Transcript