Colon Cancer: Gene >> AFAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358461
Start	7809753:7809753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.915G>T
AA Mutation	p.Lys305Asn(p.K305N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358461
Start	7843185:7843185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.500G>A
AA Mutation	p.Gly167Asp(p.G167D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358461
Start	7793689:7793689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1404G>T
AA Mutation	p.Gln468His(p.Q468H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358461
Start	7768929:7768929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2081C>A
AA Mutation	p.Pro694Gln(p.P694Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358461
Start	7768860:7768860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2150T>C
AA Mutation	p.Val717Ala(p.V717A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358461
Start	7772935:7772935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs569262471
CDS Mutation	c.1886G>A
AA Mutation	p.Arg629His(p.R629H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000358461
Start	7800464:7800464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1244G>A
AA Mutation	p.Gly415Asp(p.G415D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000358461
Start	7843225:7843225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.460G>A
AA Mutation	p.Ala154Thr(p.A154T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358461
Start	7843237:7843237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372896349
CDS Mutation	c.448C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358461
Start	7809717:7809717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143460564
CDS Mutation	c.951G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000358461
Start	7819128:7819128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.770C>G
AA Mutation	p.Ser257Ter(p.S257*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> AFAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358461
Start	7774883:7774883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1666G>C
AA Mutation	p.Gly556Arg(p.G556R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358461
Start	7800465:7800465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1243G>A
AA Mutation	p.Gly415Ser(p.G415S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358461
Start	7768990:7768990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149064401
CDS Mutation	c.2020C>T
AA Mutation	p.Arg674Trp(p.R674W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript