Colon Cancer: Gene >> MAL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309988
Start	95049678:95049678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.359G>T
AA Mutation	p.Arg120Met(p.R120M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309988
Start	95048010:95048010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.145C>G
AA Mutation	p.Pro49Ala(p.P49A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309988
Start	95049654:95049654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749751444
CDS Mutation	c.335C>T
AA Mutation	p.Thr112Met(p.T112M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000309988
Start	95047992:95047992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.127T>A
AA Mutation	p.Ser43Thr(p.S43T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309988
Start	95049601:95049601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761322906
CDS Mutation	c.282C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309988
Start	95049628:95049628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.309A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MAL

No Mutation Annotation!