Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ZMAT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311417
Start	179025195:179025195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.692G>T
AA Mutation	p.Arg231Ile(p.R231I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311417
Start	179067494:179067494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.259G>T
AA Mutation	p.Ala87Ser(p.A87S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311417
Start	179025130:179025130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.757G>A
AA Mutation	p.Val253Ile(p.V253I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311417
Start	179067704:179067704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.49C>T
AA Mutation	p.Pro17Ser(p.P17S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311417
Start	179025187:179025187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774816930
CDS Mutation	c.700C>T
AA Mutation	p.Arg234Cys(p.R234C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000311417
Start	179030915:179030915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.355C>T
AA Mutation	p.Pro119Ser(p.P119S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000311417
Start	179025177:179025177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.710C>T
AA Mutation	p.Ala237Val(p.A237V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311417
Start	179030883:179030883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138510384
CDS Mutation	c.387G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000311417
Start	179027788:179027788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147086451
CDS Mutation	c.415C>T
AA Mutation	p.Arg139Ter(p.R139*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZMAT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311417
Start	179030974:179030974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.296G>A
AA Mutation	p.Arg99Gln(p.R99Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311417
Start	179025035:179025035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.852G>T
AA Mutation	p.Glu284Asp(p.E284D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311417
Start	179025195:179025195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.692G>T
AA Mutation	p.Arg231Ile(p.R231I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000311417
Start	179025196:179025196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.691A>T
AA Mutation	p.Arg231Ter(p.R231*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript