Colon Cancer: Gene >> ANAPC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341068
Start	111769401:111769401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5725A>T
AA Mutation	p.Thr1909Ser(p.T1909S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341068
Start	111785457:111785457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4820G>A
AA Mutation	p.Arg1607Gln(p.R1607Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341068
Start	111834866:111834866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2122G>A
AA Mutation	p.Glu708Lys(p.E708K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000341068
Start	111858378:111858378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1286A>C
AA Mutation	p.Lys429Thr(p.K429T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000341068
Start	111864949:111864949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.688C>A
AA Mutation	p.Leu230Ile(p.L230I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000341068
Start	111843593:111843593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144034109
CDS Mutation	c.1859C>T
AA Mutation	p.Thr620Met(p.T620M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000341068
Start	111856833:111856833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1412T>C
AA Mutation	p.Val471Ala(p.V471A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000341068
Start	111803760:111803760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4004G>A
AA Mutation	p.Arg1335His(p.R1335H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000341068
Start	111856857:111856857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1388A>C
AA Mutation	p.Lys463Thr(p.K463T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000341068
Start	111769349:111769349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5777G>A
AA Mutation	p.Arg1926Gln(p.R1926Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000341068
Start	111794825:111794825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4366A>T
AA Mutation	p.Thr1456Ser(p.T1456S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341068
Start	111834642:111834642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2346A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341068
Start	111880820:111880820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747691768
CDS Mutation	c.6G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000341068
Start	111784370:111784370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749616796
CDS Mutation	c.4948G>T
AA Mutation	p.Glu1650Ter(p.E1650*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000341068
Start	111802487:111802487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4162C>T
AA Mutation	p.Arg1388Ter(p.R1388*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ANAPC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341068
Start	111834706:111834706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2282C>T
AA Mutation	p.Ala761Val(p.A761V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341068
Start	111794885:111794885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4306G>A
AA Mutation	p.Glu1436Lys(p.E1436K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341068
Start	111783925:111783925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5035G>T
AA Mutation	p.Asp1679Tyr(p.D1679Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript