Colon Cancer: Gene >> AKAP10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225737
Start	19936352:19936352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1401G>T
AA Mutation	p.Arg467Ser(p.R467S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000225737
Start	19962893:19962893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.266C>T
AA Mutation	p.Ala89Val(p.A89V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000225737
Start	19939748:19939748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1287G>T
AA Mutation	p.Gln429His(p.Q429H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000225737
Start	19941849:19941849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778214457
CDS Mutation	c.1038A>G
AA Mutation	p.Ile346Met(p.I346M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225737
Start	19924434:19924434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1725A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> AKAP10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225737
Start	19924442:19924442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1717G>A
AA Mutation	p.Asp573Asn(p.D573N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000225737
Start	19958199:19958199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.692G>T
AA Mutation	p.Ser231Ile(p.S231I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000225737
Start	19931909:19931909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1537C>T
AA Mutation	p.Arg513Ter(p.R513*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript