Colon Cancer: Gene >> CAMKK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324774
Start	121240720:121240720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1746G>T
AA Mutation	p.Glu582Asp(p.E582D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324774
Start	121248687:121248687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1371G>T
AA Mutation	p.Glu457Asp(p.E457D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324774
Start	121274319:121274319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201146989
CDS Mutation	c.208C>T
AA Mutation	p.Arg70Trp(p.R70W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000324774
Start	121245219:121245219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1474C>T
AA Mutation	p.Arg492Cys(p.R492C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000324774
Start	121269553:121269553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.548A>C
AA Mutation	p.Tyr183Ser(p.Y183S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000324774
Start	121255799:121255799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.802G>A
AA Mutation	p.Glu268Lys(p.E268K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000324774
Start	121274328:121274328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746435585
CDS Mutation	c.199G>A
AA Mutation	p.Gly67Ser(p.G67S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324774
Start	121255800:121255800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201031410
CDS Mutation	c.801C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324774
Start	121240762:121240762(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1704delC
AA Mutation	p.Ala569ProfsTer72(p.A569Pfs*72)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324774
Start	121240817:121240817(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1649delG
AA Mutation	p.Gly550GlufsTer7(p.G550Efs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324774
Start	121274478:121274478(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.49delC
AA Mutation	p.Gln17ArgfsTer27(p.Q17Rfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324774
Start	121274461:121274462(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.65dupG
AA Mutation	p.Arg23GlnfsTer13(p.R23Qfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CAMKK2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000324774
Start	121263937:121263937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762984197
CDS Mutation	c.628C>T
AA Mutation	p.Arg210Cys(p.R210C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324774
Start	121270942:121270942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.475T>G
AA Mutation	p.Cys159Gly(p.C159G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000324774
Start	121260317:121260317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.796+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript