Colon Cancer: Gene >> PRKCG

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000263431
Start	53892511:53892511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.689A>G
AA Mutation	p.Asn230Ser(p.N230S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263431
Start	53906714:53906714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768380642
CDS Mutation	c.1913G>A
AA Mutation	p.Arg638His(p.R638H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263431
Start	53893374:53893374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778748565
CDS Mutation	c.922C>T
AA Mutation	p.Pro308Ser(p.P308S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263431
Start	53897995:53897995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.976T>C
AA Mutation	p.Ser326Pro(p.S326P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263431
Start	53893023:53893023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.857A>T
AA Mutation	p.Tyr286Phe(p.Y286F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263431
Start	53900237:53900237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1286G>A
AA Mutation	p.Arg429His(p.R429H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263431
Start	53906750:53906750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1949C>T
AA Mutation	p.Ala650Val(p.A650V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000263431
Start	53900678:53900678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1504T>C
AA Mutation	p.Cys502Arg(p.C502R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000263431
Start	53898052:53898052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1033C>T
AA Mutation	p.Arg345Cys(p.R345C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000263431
Start	53884193:53884193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.235G>A
AA Mutation	p.Glu79Lys(p.E79K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000263431
Start	53891758:53891758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762399754
CDS Mutation	c.614G>A
AA Mutation	p.Arg205Gln(p.R205Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000263431
Start	53882562:53882562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.68G>A
AA Mutation	p.Gly23Glu(p.G23E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000263431
Start	53898016:53898016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.997G>A
AA Mutation	p.Asp333Asn(p.D333N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000263431
Start	53884208:53884208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.250G>C
AA Mutation	p.Glu84Gln(p.E84Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000263431
Start	53900427:53900427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751774653
CDS Mutation	c.1382C>T
AA Mutation	p.Ala461Val(p.A461V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263431
Start	53898042:53898042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757306727
CDS Mutation	c.1023G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263431
Start	53884219:53884219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779160754
CDS Mutation	c.261C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263431
Start	53898451:53898451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1104C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263431
Start	53898508:53898508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1161C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263431
Start	53906811:53906811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2010C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263431
Start	53882572:53882572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.78G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263431
Start	53891768:53891768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs553245210
CDS Mutation	c.624G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263431
Start	53903138:53903138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200404402
CDS Mutation	c.1641G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263431
Start	53906760:53906760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766461264
CDS Mutation	c.1959G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263431
Start	53906389:53906389(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1841delT
AA Mutation	p.Phe614SerfsTer41(p.F614Sfs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263431
Start	53882530:53882530(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.41delG
AA Mutation	p.Gly14AspfsTer12(p.G14Dfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000263431
Start	53893380:53893380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.928G>T
AA Mutation	p.Glu310Ter(p.E310*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000263431
Start	53891781:53891781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750289253
CDS Mutation	c.637C>T
AA Mutation	p.Arg213Ter(p.R213*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PRKCG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263431
Start	53892600:53892600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.778T>C
AA Mutation	p.Ser260Pro(p.S260P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263431
Start	53892577:53892577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.755G>A
AA Mutation	p.Arg252His(p.R252H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263431
Start	53900656:53900656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1482C>G
AA Mutation	p.Ile494Met(p.I494M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263431
Start	53891686:53891686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.542G>A
AA Mutation	p.Arg181His(p.R181H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263431
Start	53884193:53884193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.235G>A
AA Mutation	p.Glu79Lys(p.E79K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263431
Start	53891768:53891768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs553245210
CDS Mutation	c.624G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263431
Start	53898051:53898051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1032A>G
Mutation Classification	Silent
Feature Type	Transcript