Colon Cancer: Gene >> ZDHHC9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357166
Start	129823731:129823731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.435G>T
AA Mutation	p.Lys145Asn(p.K145N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000357166
Start	129811406:129811406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.881G>T
AA Mutation	p.Ser294Ile(p.S294I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357166
Start	129823804:129823804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.362G>A
AA Mutation	p.Arg121Gln(p.R121Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000357166
Start	129806459:129806459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1006G>A
AA Mutation	p.Glu336Lys(p.E336K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357166
Start	129829018:129829018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs77513704
CDS Mutation	c.291G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357166
Start	129812778:129812778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.717C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357166
Start	129814674:129814674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781147368
CDS Mutation	c.609C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357166
Start	129829019:129829020(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.289dupG
AA Mutation	p.Ala97GlyfsTer5(p.A97Gfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000357166
Start	129810903:129810903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.978+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ZDHHC9

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000357166
Start	129814793:129814793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754241413
CDS Mutation	c.490C>T
AA Mutation	p.Arg164Cys(p.R164C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357166
Start	129823728:129823728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.438C>A
Mutation Classification	Silent
Feature Type	Transcript