Colon Cancer: Gene >> CDK8

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000381527
Start	26385211:26385211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.515C>A
AA Mutation	p.Ala172Asp(p.A172D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381527
Start	26403966:26403966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1280C>T
AA Mutation	p.Pro427Leu(p.P427L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381527
Start	26353761:26353761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.337G>A
AA Mutation	p.Ala113Thr(p.A113T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000381527
Start	26401470:26401470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1115A>G
AA Mutation	p.Asn372Ser(p.N372S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381527
Start	26349167:26349167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.300T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381527
Start	26382846:26382846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.489T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000381527
Start	26401309:26401309(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1076delT
AA Mutation	p.Leu359Ter(p.L359*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000381527
Start	26337591:26337591(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.156delA
AA Mutation	p.Lys52AsnfsTer3(p.K52Nfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000381527
Start	26385228:26385228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.532C>T
AA Mutation	p.Arg178Ter(p.R178*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000381527
Start	26396313:26396315(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.819_821delGCC
AA Mutation	p.Met273_Pro274delinsIle(p.M273_P274delinsI)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CDK8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381527
Start	26382828:26382828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.471T>G
AA Mutation	p.Ile157Met(p.I157M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381527
Start	26393418:26393418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.698T>G
AA Mutation	p.Ile233Arg(p.I233R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381527
Start	26393430:26393430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.710G>A
AA Mutation	p.Arg237Gln(p.R237Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000381527
Start	26400486:26400486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.967C>T
AA Mutation	p.Arg323Ter(p.R323*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000381527
Start	26349183:26349184(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.315+2dupT
Mutation Classification	Splice_Site
Feature Type	Transcript