Colon Cancer: Gene >> AKAP8L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397410
Start	15401446:15401446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.520G>A
AA Mutation	p.Asp174Asn(p.D174N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397410
Start	15399315:15399315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1144C>A
AA Mutation	p.Arg382Ser(p.R382S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397410
Start	15397154:15397154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1532G>A
AA Mutation	p.Arg511His(p.R511H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000397410
Start	15401472:15401472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747313272
CDS Mutation	c.494G>A
AA Mutation	p.Arg165His(p.R165H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000397410
Start	15397589:15397589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1336C>A
AA Mutation	p.Leu446Ile(p.L446I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000397410
Start	15403544:15403544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758338472
CDS Mutation	c.293G>A
AA Mutation	p.Arg98His(p.R98H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397410
Start	15401017:15401017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748554800
CDS Mutation	c.843C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397410
Start	15401393:15401393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.573G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397410
Start	15397780:15397780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1233G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000397410
Start	15397518:15397518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1405+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000397410
Start	15380395:15380397(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs775490570
CDS Mutation	c.1666_1668delGAG
AA Mutation	p.Glu556del(p.E556del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> AKAP8L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397410
Start	15403601:15403601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.236A>T
AA Mutation	p.Asn79Ile(p.N79I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397410
Start	15400858:15400858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.920G>A
AA Mutation	p.Gly307Asp(p.G307D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397410
Start	15399322:15399322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1137G>A
Mutation Classification	Silent
Feature Type	Transcript