Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> EMD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369842
Start	154380768:154380768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.415C>A
AA Mutation	p.Leu139Ile(p.L139I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369842
Start	154379753:154379753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.146C>T
AA Mutation	p.Ser49Leu(p.S49L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369842
Start	154381094:154381094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782057378
CDS Mutation	c.662G>A
AA Mutation	p.Arg221His(p.R221H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369842
Start	154381093:154381093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.661C>T
AA Mutation	p.Arg221Cys(p.R221C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369842
Start	154380760:154380760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.407A>C
AA Mutation	p.Asp136Ala(p.D136A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369842
Start	154381042:154381042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.610C>A
AA Mutation	p.Arg204Ser(p.R204S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> EMD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369842
Start	154380353:154380353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782768362
CDS Mutation	c.385G>A
AA Mutation	p.Ala129Thr(p.A129T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369842
Start	154381184:154381184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.752G>T
AA Mutation	p.Gly251Val(p.G251V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369842
Start	154379790:154379790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.183C>A
AA Mutation	p.Phe61Leu(p.F61L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript