Colon Cancer: Gene >> MAF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393350
Start	79599676:79599676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.227C>T
AA Mutation	p.Pro76Leu(p.P76L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000393350
Start	79599509:79599509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.394G>A
AA Mutation	p.Ala132Thr(p.A132T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000393350
Start	79599589:79599589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759815012
CDS Mutation	c.314C>T
AA Mutation	p.Ala105Val(p.A105V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000393350
Start	79599845:79599845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.58G>A
AA Mutation	p.Glu20Lys(p.E20K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000393350
Start	79598888:79598888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1015C>T
AA Mutation	p.Arg339Cys(p.R339C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000393350
Start	79598974:79598974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.929T>C
AA Mutation	p.Val310Ala(p.V310A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000393350
Start	79599061:79599061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.842T>G
AA Mutation	p.Val281Gly(p.V281G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000393350
Start	79599610:79599610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.293C>A
AA Mutation	p.Pro98Gln(p.P98Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000393350
Start	79598806:79598806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1097C>T
AA Mutation	p.Pro366Leu(p.P366L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393350
Start	79599705:79599705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.198G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000393350
Start	79599697:79599697(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.206delC
AA Mutation	p.Pro69LeufsTer26(p.P69Lfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000393350
Start	79598904:79598906(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.997_999delGAG
AA Mutation	p.Glu333del(p.E333del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	start_lost
Transcription ID	ENST00000393350
Start	79599902:79599902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1A>G
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MAF

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393350
Start	79599588:79599588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754156981
CDS Mutation	c.315G>T
Mutation Classification	Silent
Feature Type	Transcript