Colon Cancer: Gene >> ANXA7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372919
Start	73380195:73380195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770697765
CDS Mutation	c.991C>T
AA Mutation	p.Arg331Cys(p.R331C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372919
Start	73379921:73379921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778139210
CDS Mutation	c.1189C>T
AA Mutation	p.Arg397Cys(p.R397C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372919
Start	73379909:73379909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765172371
CDS Mutation	c.1201G>A
AA Mutation	p.Gly401Arg(p.G401R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372919
Start	73376187:73376187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146521289
CDS Mutation	c.1375G>A
AA Mutation	p.Ala459Thr(p.A459T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372919
Start	73397171:73397171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.363A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ANXA7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372919
Start	73383606:73383606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769213073
CDS Mutation	c.784G>A
AA Mutation	p.Asp262Asn(p.D262N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372919
Start	73380194:73380194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs10159690
CDS Mutation	c.992G>A
AA Mutation	p.Arg331His(p.R331H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript