Colon Cancer: Gene >> ZNF768

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380412
Start	30524831:30524831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1309C>G
AA Mutation	p.Arg437Gly(p.R437G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380412
Start	30525214:30525214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.926G>A
AA Mutation	p.Arg309His(p.R309H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380412
Start	30525554:30525554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.586G>T
AA Mutation	p.Asp196Tyr(p.D196Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380412
Start	30524653:30524653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1487G>A
AA Mutation	p.Arg496His(p.R496H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000380412
Start	30525728:30525728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.412C>T
AA Mutation	p.Arg138Trp(p.R138W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000380412
Start	30525286:30525286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.854G>A
AA Mutation	p.Gly285Asp(p.G285D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000380412
Start	30525433:30525433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.707T>C
AA Mutation	p.Leu236Pro(p.L236P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000380412
Start	30525178:30525178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.962G>A
AA Mutation	p.Arg321His(p.R321H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380412
Start	30524679:30524679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1461C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380412
Start	30524772:30524772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1368C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF768

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380412
Start	30525619:30525619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.521C>T
AA Mutation	p.Ala174Val(p.A174V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380412
Start	30525838:30525838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.302C>T
AA Mutation	p.Ala101Val(p.A101V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript