Colon Cancer: Gene >> APAF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000551964
Start	98662541:98662541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.796G>T
AA Mutation	p.Asp266Tyr(p.D266Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000551964
Start	98666296:98666296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201872620
CDS Mutation	c.1301G>A
AA Mutation	p.Arg434His(p.R434H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000551964
Start	98659309:98659309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.676C>T
AA Mutation	p.Arg226Cys(p.R226C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000551964
Start	98715446:98715446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2978A>T
AA Mutation	p.Asn993Ile(p.N993I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000551964
Start	98699442:98699442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2339G>T
AA Mutation	p.Ser780Ile(p.S780I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000551964
Start	98715508:98715508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745664662
CDS Mutation	c.3040G>A
AA Mutation	p.Asp1014Asn(p.D1014N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000551964
Start	98706504:98706504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139940389
CDS Mutation	c.2615G>A
AA Mutation	p.Arg872His(p.R872H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000551964
Start	98666277:98666277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1282C>T
AA Mutation	p.Arg428Trp(p.R428W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000551964
Start	98671581:98671581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1655G>A
AA Mutation	p.Gly552Glu(p.G552E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000551964
Start	98699468:98699468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2365A>T
AA Mutation	p.Asn789Tyr(p.N789Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000551964
Start	98671017:98671017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1539A>C
AA Mutation	p.Lys513Asn(p.K513N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000551964
Start	98665584:98665584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.987A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000551964
Start	98677443:98677443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144715006
CDS Mutation	c.1812G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000551964
Start	98683154:98683154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2058T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000551964
Start	98667563:98667563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1413T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000551964
Start	98671639:98671639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755872148
CDS Mutation	c.1713G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000551964
Start	98699419:98699419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368374940
CDS Mutation	c.2316G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000551964
Start	98649593:98649593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.435T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000551964
Start	98699461:98699461(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2358delC
AA Mutation	p.Phe787SerfsTer2(p.F787Sfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000551964
Start	98671051:98671051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1573G>T
AA Mutation	p.Glu525Ter(p.E525*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000551964
Start	98671657:98671657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1731T>G
AA Mutation	p.Tyr577Ter(p.Y577*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000551964
Start	98732437:98732438(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3622dupG
AA Mutation	p.Glu1208GlyfsTer14(p.E1208Gfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> APAF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000551964
Start	98665607:98665607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1010G>A
AA Mutation	p.Arg337His(p.R337H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000551964
Start	98666263:98666264(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1270_1271delTT
AA Mutation	p.Leu424IlefsTer3(p.L424Ifs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000551964
Start	98680331:98680331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1975G>T
AA Mutation	p.Glu659Ter(p.E659*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript