Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CDC6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000209728
Start	40291265:40291265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.386A>G
AA Mutation	p.Glu129Gly(p.E129G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000209728
Start	40291519:40291519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757198932
CDS Mutation	c.511C>T
AA Mutation	p.Arg171Trp(p.R171W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000209728
Start	40300946:40300946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1368C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000209728
Start	40291132:40291132(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.257delC
AA Mutation	p.Pro86LeufsTer17(p.P86Lfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CDC6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000209728
Start	40291160:40291160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762281243
CDS Mutation	c.281G>A
AA Mutation	p.Arg94Gln(p.R94Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000209728
Start	40291537:40291537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.529A>T
AA Mutation	p.Arg177Trp(p.R177W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000209728
Start	40300982:40300982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1404G>T
AA Mutation	p.Leu468Phe(p.L468F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000209728
Start	40296739:40296739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1221C>T
Mutation Classification	Silent
Feature Type	Transcript