Colon Cancer: Gene >> HVCN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242607
Start	110661432:110661432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.38C>T
AA Mutation	p.Ala13Val(p.A13V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000242607
Start	110651265:110651265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.595G>T
AA Mutation	p.Gly199Cys(p.G199C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000242607
Start	110651250:110651250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.610C>A
AA Mutation	p.Leu204Ile(p.L204I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000242607
Start	110650215:110650215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.709C>A
AA Mutation	p.Gln237Lys(p.Q237K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000242607
Start	110651331:110651331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781358524
CDS Mutation	c.529G>A
AA Mutation	p.Val177Met(p.V177M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000242607
Start	110650206:110650206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779165493
CDS Mutation	c.718G>A
AA Mutation	p.Ala240Thr(p.A240T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000242607
Start	110651238:110651238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.622C>T
AA Mutation	p.Arg208Trp(p.R208W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000242607
Start	110661304:110661304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.166C>G
AA Mutation	p.Gln56Glu(p.Q56E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000242607
Start	110650248:110650248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772902585
CDS Mutation	c.676C>T
AA Mutation	p.Arg226Trp(p.R226W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242607
Start	110651308:110651308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.552C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242607
Start	110651332:110651332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373217560
CDS Mutation	c.528C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242607
Start	110661278:110661278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759164458
CDS Mutation	c.192C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HVCN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242607
Start	110655296:110655296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.349C>T
AA Mutation	p.Leu117Phe(p.L117F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000242607
Start	110651225:110651225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.635T>G
AA Mutation	p.Ile212Ser(p.I212S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript