Colon Cancer: Gene >> DYRK1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323039
Start	39827301:39827301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753581092
CDS Mutation	c.1079C>T
AA Mutation	p.Thr360Met(p.T360M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000323039
Start	39828377:39828377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.727G>A
AA Mutation	p.Glu243Lys(p.E243K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000323039
Start	39825794:39825794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773857931
CDS Mutation	c.1811C>T
AA Mutation	p.Pro604Leu(p.P604L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000323039
Start	39828460:39828460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.644G>A
AA Mutation	p.Arg215Gln(p.R215Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000323039
Start	39827634:39827634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.830G>A
AA Mutation	p.Arg277His(p.R277H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000323039
Start	39830413:39830413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.334G>A
AA Mutation	p.Glu112Lys(p.E112K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323039
Start	39828438:39828438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.666C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323039
Start	39831853:39831853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs182863590
CDS Mutation	c.15G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323039
Start	39827378:39827378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146996483
CDS Mutation	c.1002C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323039
Start	39831808:39831808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142943294
CDS Mutation	c.60G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323039
Start	39830525:39830525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774335838
CDS Mutation	c.222G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323039
Start	39829929:39829929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.471G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000323039
Start	39825972:39825972(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1633delC
AA Mutation	p.Gln545SerfsTer19(p.Q545Sfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000323039
Start	39825971:39825972(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs775499198
CDS Mutation	c.1633dupC
AA Mutation	p.Gln545ProfsTer30(p.Q545Pfs*30)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> DYRK1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323039
Start	39827307:39827307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761527610
CDS Mutation	c.1073G>A
AA Mutation	p.Arg358Gln(p.R358Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000323039
Start	39828349:39828349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746933234
CDS Mutation	c.755G>A
AA Mutation	p.Arg252His(p.R252H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323039
Start	39828450:39828450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538308215
CDS Mutation	c.654G>A
Mutation Classification	Silent
Feature Type	Transcript