Colon Cancer: Gene >> CDK19

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368911
Start	110667454:110667454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.436T>C
AA Mutation	p.Trp146Arg(p.W146R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368911
Start	110627031:110627031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.761G>A
AA Mutation	p.Arg254Gln(p.R254Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368911
Start	110667556:110667556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.334C>T
AA Mutation	p.Arg112Cys(p.R112C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368911
Start	110626806:110626806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.830C>A
AA Mutation	p.Pro277His(p.P277H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368911
Start	110638653:110638653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.510A>C
AA Mutation	p.Lys170Asn(p.K170N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368911
Start	110627032:110627032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.760C>T
AA Mutation	p.Arg254Trp(p.R254W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368911
Start	110621224:110621224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148540500
CDS Mutation	c.1257C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368911
Start	110627102:110627102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757607893
CDS Mutation	c.690G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CDK19

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368911
Start	110632077:110632077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.599G>A
AA Mutation	p.Arg200Gln(p.R200Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368911
Start	110627103:110627103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.689C>T
AA Mutation	p.Ser230Leu(p.S230L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript