Colon Cancer: Gene >> ANAPC4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315368
Start	25380428:25380428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.184G>A
AA Mutation	p.Glu62Lys(p.E62K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315368
Start	25380377:25380377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.133T>G
AA Mutation	p.Leu45Val(p.L45V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315368
Start	25415495:25415495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1856A>C
AA Mutation	p.Lys619Thr(p.K619T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000315368
Start	25388736:25388736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.463A>C
AA Mutation	p.Ile155Leu(p.I155L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315368
Start	25396670:25396670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs34015658
CDS Mutation	c.1068G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained;inframe_insertion
Transcription ID	ENST00000315368
Start	25396759:25396760(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1157_1158insAAATTAGTATCATGA
AA Mutation	p.Ile386_Glu387insAsnTerTyrHisAsp(p.I386_E387insN*YHD)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000315368
Start	25403004:25403005(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1254dupT
AA Mutation	p.Arg419SerfsTer21(p.R419Sfs*21)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000315368
Start	25417644:25417645(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2104_2105insATATAATTTTAG
AA Mutation	p.Thr702delinsAsnIleIleLeuAla(p.T702delinsNIILA)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ANAPC4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315368
Start	25418171:25418171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2216G>A
AA Mutation	p.Arg739His(p.R739H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315368
Start	25415530:25415530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1891G>C
AA Mutation	p.Val631Leu(p.V631L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315368
Start	25403011:25403011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201488708
CDS Mutation	c.1255C>T
AA Mutation	p.Arg419Trp(p.R419W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000315368
Start	25414494:25414494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1714T>A
AA Mutation	p.Phe572Ile(p.F572I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000315368
Start	25416538:25416538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2015C>A
AA Mutation	p.Ser672Tyr(p.S672Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000315368
Start	25383275:25383275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.250C>T
AA Mutation	p.Leu84Phe(p.L84F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000315368
Start	25396761:25396761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535292691
CDS Mutation	c.1159G>A
AA Mutation	p.Glu387Lys(p.E387K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000315368
Start	25406841:25406841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1330G>T
AA Mutation	p.Asp444Tyr(p.D444Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000315368
Start	25418264:25418264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2309A>C
AA Mutation	p.Lys770Thr(p.K770T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript