Colon Cancer: Gene >> PRKACG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377276
Start	69013466:69013466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.627G>T
AA Mutation	p.Glu209Asp(p.E209D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377276
Start	69013655:69013655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.438C>A
AA Mutation	p.Phe146Leu(p.F146L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377276
Start	69013084:69013084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768219024
CDS Mutation	c.1009C>T
AA Mutation	p.Arg337Trp(p.R337W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377276
Start	69013814:69013814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.279G>T
AA Mutation	p.Lys93Asn(p.K93N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377276
Start	69013639:69013639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.454G>A
AA Mutation	p.Val152Ile(p.V152I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377276
Start	69013198:69013198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.895G>A
AA Mutation	p.Ala299Thr(p.A299T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000377276
Start	69013978:69013978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.115G>A
AA Mutation	p.Ala39Thr(p.A39T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000377276
Start	69013180:69013180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.913G>A
AA Mutation	p.Ala305Thr(p.A305T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000377276
Start	69013779:69013779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.314T>C
AA Mutation	p.Val105Ala(p.V105A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377276
Start	69013493:69013493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.600C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377276
Start	69014063:69014063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.30C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377276
Start	69013487:69013487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.606C>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PRKACG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377276
Start	69014041:69014041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.52G>A
AA Mutation	p.Glu18Lys(p.E18K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377276
Start	69013493:69013493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.600C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377276
Start	69013961:69013961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.132C>T
Mutation Classification	Silent
Feature Type	Transcript