Colon Cancer: Gene >> CDKAL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274695
Start	21201132:21201132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1406C>G
AA Mutation	p.Ala469Gly(p.A469G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000274695
Start	20781166:20781166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.539G>A
AA Mutation	p.Gly180Asp(p.G180D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000274695
Start	20739581:20739581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149431105
CDS Mutation	c.434G>A
AA Mutation	p.Arg145His(p.R145H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000274695
Start	20781201:20781201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.574G>A
AA Mutation	p.Ala192Thr(p.A192T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274695
Start	20546458:20546458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759073576
CDS Mutation	c.108G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000274695
Start	21231015:21231015(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1722delT
AA Mutation	p.Phe574LeufsTer39(p.F574Lfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000274695
Start	21065200:21065201(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1213dupA
AA Mutation	p.Met405AsnfsTer27(p.M405Nfs*27)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000274695
Start	20739576:20739577(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.431dupC
AA Mutation	p.Arg145SerfsTer6(p.R145Sfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000274695
Start	20758638:20758639(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.512_513insAAAAAATATCCTA
AA Mutation	p.Gly173AsnfsTer4(p.G173Nfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000274695
Start	20781199:20781200(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.573_574insAACA
AA Mutation	p.Ala192AsnfsTer10(p.A192Nfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CDKAL1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274695
Start	20955456:20955456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748807478
CDS Mutation	c.780G>A
Mutation Classification	Silent
Feature Type	Transcript