Colon Cancer: Gene >> CDKL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000429927
Start	75597177:75597177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1080A>C
AA Mutation	p.Lys360Asn(p.K360N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000429927
Start	75607279:75607279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755711267
CDS Mutation	c.446G>A
AA Mutation	p.Arg149Gln(p.R149Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000429927
Start	75625942:75625942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.47G>A
AA Mutation	p.Gly16Glu(p.G16E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000429927
Start	75607349:75607349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.376G>T
AA Mutation	p.Asp126Tyr(p.D126Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000429927
Start	75597130:75597130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1127G>A
AA Mutation	p.Ser376Asn(p.S376N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000429927
Start	75607295:75607295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.430G>A
AA Mutation	p.Asp144Asn(p.D144N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000429927
Start	75614396:75614396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.222A>C
AA Mutation	p.Lys74Asn(p.K74N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000429927
Start	75596991:75596991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1266T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000429927
Start	75597162:75597162(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1095delA
AA Mutation	p.Ala366LeufsTer23(p.A366Lfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000429927
Start	75597153:75597153(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1104delA
AA Mutation	p.Gly369AlafsTer20(p.G369Afs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CDKL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000429927
Start	75597053:75597053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142919399
CDS Mutation	c.1204G>A
AA Mutation	p.Val402Met(p.V402M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript