Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MAP2K5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000178640
Start	67563304:67563304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.206G>A
AA Mutation	p.Arg69Gln(p.R69Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000178640
Start	67543417:67543417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.82G>A
AA Mutation	p.Ala28Thr(p.A28T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000178640
Start	67585910:67585910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532904399
CDS Mutation	c.343C>T
AA Mutation	p.Arg115Trp(p.R115W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000178640
Start	67580821:67580821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771473899
CDS Mutation	c.320G>T
AA Mutation	p.Arg107Ile(p.R107I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MAP2K5

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000178640
Start	67693567:67693567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.971C>T
AA Mutation	p.Ala324Val(p.A324V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000178640
Start	67543375:67543375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.40A>C
AA Mutation	p.Asn14His(p.N14H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000178640
Start	67806727:67806727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762268601
CDS Mutation	c.1324C>T
AA Mutation	p.Arg442Trp(p.R442W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript