Colon Cancer: Gene >> AKAP8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269701
Start	15372865:15372865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.847C>T
AA Mutation	p.Arg283Trp(p.R283W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269701
Start	15373000:15373000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.712C>T
AA Mutation	p.Pro238Ser(p.P238S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000269701
Start	15373200:15373200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.512G>A
AA Mutation	p.Ser171Asn(p.S171N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000269701
Start	15371975:15371975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1015T>G
AA Mutation	p.Ser339Ala(p.S339A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000269701
Start	15373997:15373997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371961765
CDS Mutation	c.160G>A
AA Mutation	p.Gly54Ser(p.G54S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000269701
Start	15360871:15360871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773404765
CDS Mutation	c.1504G>A
AA Mutation	p.Val502Met(p.V502M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000269701
Start	15372335:15372335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.874G>T
AA Mutation	p.Gly292Trp(p.G292W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000269701
Start	15373081:15373081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532876878
CDS Mutation	c.631G>A
AA Mutation	p.Val211Met(p.V211M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269701
Start	15355080:15355080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538149553
CDS Mutation	c.1914C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269701
Start	15373244:15373244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773627639
CDS Mutation	c.468C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269701
Start	15368309:15368309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778010401
CDS Mutation	c.1086C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269701
Start	15373193:15373193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.519C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000269701
Start	15372220:15372220(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.989delA
AA Mutation	p.Asn330MetfsTer38(p.N330Mfs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> AKAP8

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269701
Start	15373244:15373244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773627639
CDS Mutation	c.468C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269701
Start	15373100:15373100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.612C>T
Mutation Classification	Silent
Feature Type	Transcript