Colon Cancer: Gene >> PKN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370521
Start	88741091:88741091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200490316
CDS Mutation	c.152G>A
AA Mutation	p.Arg51Gln(p.R51Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370521
Start	88807433:88807433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1924G>A
AA Mutation	p.Glu642Lys(p.E642K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370521
Start	88771706:88771706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.812T>C
AA Mutation	p.Leu271Ser(p.L271S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370521
Start	88805989:88805989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1775A>C
AA Mutation	p.Glu592Ala(p.E592A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370521
Start	88805545:88805545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1550G>T
AA Mutation	p.Trp517Leu(p.W517L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370521
Start	88805508:88805508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1513C>A
AA Mutation	p.Leu505Ile(p.L505I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000370521
Start	88771805:88771805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.911C>T
AA Mutation	p.Thr304Ile(p.T304I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000370521
Start	88804395:88804395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1286G>A
AA Mutation	p.Arg429His(p.R429H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370521
Start	88786129:88786129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535484606
CDS Mutation	c.1197C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370521
Start	88833367:88833367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2874T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370521
Start	88807565:88807565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1971C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370521
Start	88741165:88741165(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.232delA
AA Mutation	p.Ser78ValfsTer5(p.S78Vfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000370521
Start	88833374:88833374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2881C>T
AA Mutation	p.Arg961Ter(p.R961*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000370521
Start	88832743:88832743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2563-1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PKN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370521
Start	88805997:88805997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1783G>T
AA Mutation	p.Val595Phe(p.V595F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370521
Start	88804514:88804514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1405C>A
AA Mutation	p.Gln469Lys(p.Q469K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370521
Start	88805983:88805983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1769C>T
AA Mutation	p.Ser590Phe(p.S590F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370521
Start	88771450:88771450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.652C>T
AA Mutation	p.Arg218Trp(p.R218W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370521
Start	88771746:88771746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.852G>T
AA Mutation	p.Lys284Asn(p.K284N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370521
Start	88771840:88771840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.946A>C
AA Mutation	p.Asn316His(p.N316H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript