Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CRADD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332896
Start	93678947:93678947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.173T>C
AA Mutation	p.Leu58Pro(p.L58P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000332896
Start	93850224:93850224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.553C>T
AA Mutation	p.Arg185Trp(p.R185W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000332896
Start	93678929:93678929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768737669
CDS Mutation	c.155G>A
AA Mutation	p.Arg52Gln(p.R52Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332896
Start	93850190:93850190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.519G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332896
Start	93850136:93850136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774580724
CDS Mutation	c.465C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CRADD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332896
Start	93850144:93850144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752845581
CDS Mutation	c.473C>T
AA Mutation	p.Ser158Leu(p.S158L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000332896
Start	93850062:93850062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373657793
CDS Mutation	c.391T>C
AA Mutation	p.Trp131Arg(p.W131R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000332896
Start	93850185:93850185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.514G>A
AA Mutation	p.Gly172Arg(p.G172R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332896
Start	93678990:93678990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.216C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332896
Start	93679026:93679026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.252G>A
Mutation Classification	Silent
Feature Type	Transcript