Colon Cancer: Gene >> AKAP5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320636
Start	64469667:64469667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1273C>A
AA Mutation	p.Leu425Ile(p.L425I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000320636
Start	64468678:64468678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.284C>T
AA Mutation	p.Ser95Leu(p.S95L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000320636
Start	64469247:64469247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.853C>G
AA Mutation	p.Leu285Val(p.L285V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000320636
Start	64469098:64469098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.704C>T
AA Mutation	p.Thr235Met(p.T235M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320636
Start	64468952:64468952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.558C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000320636
Start	64469099:64469099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767093043
CDS Mutation	c.705G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000320636
Start	64468621:64468621(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.232delG
AA Mutation	p.Ala78ProfsTer9(p.A78Pfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> AKAP5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000320636
Start	64469565:64469565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1171C>G
AA Mutation	p.Leu391Val(p.L391V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000320636
Start	64468802:64468802(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.412delA
AA Mutation	p.Arg138GlyfsTer8(p.R138Gfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript