Colon Cancer: Gene >> CSNK1D

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314028
Start	82255472:82255472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.293G>T
AA Mutation	p.Arg98Met(p.R98M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000314028
Start	82253237:82253237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.344G>A
AA Mutation	p.Arg115His(p.R115H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000314028
Start	82251443:82251443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.821G>A
AA Mutation	p.Arg274Gln(p.R274Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000314028
Start	82253102:82253102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.479G>C
AA Mutation	p.Arg160Pro(p.R160P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000314028
Start	82255480:82255480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.285C>A
AA Mutation	p.Phe95Leu(p.F95L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000314028
Start	82252458:82252458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765104663
CDS Mutation	c.712G>A
AA Mutation	p.Glu238Lys(p.E238K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000314028
Start	82251429:82251429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751091452
CDS Mutation	c.835C>T
AA Mutation	p.Arg279Cys(p.R279C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314028
Start	82253137:82253137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145619785
CDS Mutation	c.444C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314028
Start	82253044:82253044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146479130
CDS Mutation	c.537C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000314028
Start	82249459:82249459(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1029delC
AA Mutation	p.Thr344HisfsTer26(p.T344Hfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000314028
Start	82249000:82249000(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1072delC
AA Mutation	p.Arg358GlyfsTer12(p.R358Gfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CSNK1D

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314028
Start	82265775:82265775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.98A>C
AA Mutation	p.Glu33Ala(p.E33A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000314028
Start	82251525:82251525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.739G>A
AA Mutation	p.Glu247Lys(p.E247K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314028
Start	82249546:82249546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.942G>A
Mutation Classification	Silent
Feature Type	Transcript