Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MOG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376917
Start	29659519:29659519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781193948
CDS Mutation	c.289C>T
AA Mutation	p.Arg97Trp(p.R97W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376917
Start	29666194:29666194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.479C>T
AA Mutation	p.Ala160Val(p.A160V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376917
Start	29670356:29670356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.668C>T
AA Mutation	p.Ala223Val(p.A223V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376917
Start	29659411:29659411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.181G>A
AA Mutation	p.Ala61Thr(p.A61T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376917
Start	29659652:29659652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.422A>C
AA Mutation	p.Glu141Ala(p.E141A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MOG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376917
Start	29667915:29667915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.583C>T
AA Mutation	p.Arg195Trp(p.R195W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376917
Start	29659449:29659449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.219C>A
AA Mutation	p.Phe73Leu(p.F73L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000376917
Start	29667905:29667905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.573G>T
AA Mutation	p.Glu191Asp(p.E191D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376917
Start	29666195:29666195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148630553
CDS Mutation	c.480G>A
Mutation Classification	Silent
Feature Type	Transcript