Colon Cancer: Gene >> COG8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306875
Start	69334817:69334817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200476177
CDS Mutation	c.1117C>T
AA Mutation	p.Arg373Trp(p.R373W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306875
Start	69334889:69334889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1045T>C
AA Mutation	p.Cys349Arg(p.C349R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306875
Start	69335225:69335225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760792801
CDS Mutation	c.709G>A
AA Mutation	p.Val237Ile(p.V237I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306875
Start	69334797:69334797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530066629
CDS Mutation	c.1137C>A
AA Mutation	p.Phe379Leu(p.F379L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000306875
Start	69334544:69334544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1390G>C
AA Mutation	p.Ala464Pro(p.A464P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000306875
Start	69334711:69334711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1223C>A
AA Mutation	p.Thr408Asn(p.T408N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306875
Start	69335109:69335109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147094162
CDS Mutation	c.825C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000306875
Start	69336639:69336639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.451G>T
AA Mutation	p.Glu151Ter(p.E151*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> COG8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306875
Start	69335114:69335114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.820A>G
AA Mutation	p.Thr274Ala(p.T274A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306875
Start	69331049:69331049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1629G>A
Mutation Classification	Silent
Feature Type	Transcript