Colon Cancer: Gene >> PRKCA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000413366
Start	66742679:66742679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1443C>A
AA Mutation	p.Asp481Glu(p.D481E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000413366
Start	66732776:66732776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1007T>G
AA Mutation	p.Leu336Arg(p.L336R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000413366
Start	66641428:66641428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.362T>C
AA Mutation	p.Leu121Pro(p.L121P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000413366
Start	66645387:66645387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748433014
CDS Mutation	c.405C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000413366
Start	66303013:66303013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576353595
CDS Mutation	c.162C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000413366
Start	66788866:66788866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1741C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000413366
Start	66741692:66741692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772638644
CDS Mutation	c.1356C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000413366
Start	66641357:66641357(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.294delC
AA Mutation	p.Arg99GlyfsTer32(p.R99Gfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000413366
Start	66788883:66788883(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1762delG
AA Mutation	p.Glu588ArgfsTer4(p.E588Rfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000413366
Start	66688330:66688330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761303069
CDS Mutation	c.715C>T
AA Mutation	p.Arg239Ter(p.R239*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PRKCA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000413366
Start	66641412:66641412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.346G>A
AA Mutation	p.Asp116Asn(p.D116N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000413366
Start	66803913:66803913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140466753
CDS Mutation	c.1895G>A
AA Mutation	p.Arg632Gln(p.R632Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000413366
Start	66735533:66735533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758765811
CDS Mutation	c.1101C>A
Mutation Classification	Silent
Feature Type	Transcript