Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MIP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257979
Start	56453106:56453106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.572C>A
AA Mutation	p.Pro191His(p.P191H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000257979
Start	56454415:56454415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs77163805
CDS Mutation	c.199G>A
AA Mutation	p.Val67Ile(p.V67I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000257979
Start	56453704:56453704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748257915
CDS Mutation	c.412A>G
AA Mutation	p.Thr138Ala(p.T138A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000257979
Start	56453689:56453689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.427C>T
AA Mutation	p.Leu143Phe(p.L143F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000257979
Start	56453692:56453692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.424G>A
AA Mutation	p.Val142Met(p.V142M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MIP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257979
Start	56451372:56451372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.700C>A
AA Mutation	p.Leu234Met(p.L234M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000257979
Start	56454474:56454474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.140C>T
AA Mutation	p.Ala47Val(p.A47V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257979
Start	56451372:56451372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.700C>T
Mutation Classification	Silent
Feature Type	Transcript