Colon Cancer: Gene >> PRKAA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397128
Start	40767484:40767484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.803C>T
AA Mutation	p.Ala268Val(p.A268V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397128
Start	40764976:40764976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1084C>A
AA Mutation	p.Leu362Ile(p.L362I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397128
Start	40764904:40764904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1156C>T
AA Mutation	p.Arg386Cys(p.R386C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000397128
Start	40765190:40765190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.870G>T
AA Mutation	p.Glu290Asp(p.E290D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000397128
Start	40777520:40777520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.194G>A
AA Mutation	p.Ser65Asn(p.S65N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000397128
Start	40771728:40771728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.499G>A
AA Mutation	p.Ala167Thr(p.A167T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000397128
Start	40764903:40764903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1157G>A
AA Mutation	p.Arg386His(p.R386H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000397128
Start	40763020:40763020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1438G>A
AA Mutation	p.Glu480Lys(p.E480K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397128
Start	40777576:40777576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.138T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397128
Start	40798127:40798127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.63G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000397128
Start	40767631:40767631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.656T>A
AA Mutation	p.Leu219Ter(p.L219*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000397128
Start	40777587:40777587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.128-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PRKAA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397128
Start	40765007:40765007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1053C>A
AA Mutation	p.Phe351Leu(p.F351L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript