Colon Cancer: Gene >> DYRK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344096
Start	67649928:67649928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.181G>A
AA Mutation	p.Ala61Thr(p.A61T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344096
Start	67658649:67658649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749972090
CDS Mutation	c.1742C>T
AA Mutation	p.Ala581Val(p.A581V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000344096
Start	67657470:67657470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.563C>T
AA Mutation	p.Ala188Val(p.A188V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000344096
Start	67657680:67657680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.773G>A
AA Mutation	p.Arg258His(p.R258H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000344096
Start	67658040:67658040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543503984
CDS Mutation	c.1133G>A
AA Mutation	p.Arg378His(p.R378H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344096
Start	67657258:67657258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376315832
CDS Mutation	c.351G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344096
Start	67657993:67657993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1086C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344096
Start	67657240:67657240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.333T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344096
Start	67657960:67657960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762603987
CDS Mutation	c.1053C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344096
Start	67658404:67658404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1497G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344096
Start	67657330:67657330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.423G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000344096
Start	67657401:67657401(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.498delA
AA Mutation	p.Lys166AsnfsTer21(p.K166Nfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DYRK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344096
Start	67658440:67658440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777442529
CDS Mutation	c.1533C>A
AA Mutation	p.Phe511Leu(p.F511L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript