Colon Cancer: Gene >> AKAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337714
Start	57106461:57106461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.997A>G
AA Mutation	p.Arg333Gly(p.R333G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337714
Start	57116179:57116179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368765400
CDS Mutation	c.2350G>A
AA Mutation	p.Glu784Lys(p.E784K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000337714
Start	57114598:57114598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2243C>A
AA Mutation	p.Ser748Tyr(p.S748Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000337714
Start	57106585:57106585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139291295
CDS Mutation	c.1121G>A
AA Mutation	p.Arg374His(p.R374H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337714
Start	57106007:57106007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.543C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> AKAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337714
Start	57106315:57106315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781062994
CDS Mutation	c.851C>T
AA Mutation	p.Ala284Val(p.A284V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337714
Start	57106957:57106957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1493T>C
AA Mutation	p.Val498Ala(p.V498A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript