Colon Cancer: Gene >> ANXA5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296511
Start	121683389:121683389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.278C>T
AA Mutation	p.Ala93Val(p.A93V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296511
Start	121678438:121678438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780076315
CDS Mutation	c.451C>T
AA Mutation	p.Arg151Trp(p.R151W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296511
Start	121684717:121684717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.149G>A
AA Mutation	p.Arg50His(p.R50H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296511
Start	121670000:121670000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145513784
CDS Mutation	c.734G>A
AA Mutation	p.Arg245Gln(p.R245Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296511
Start	121681738:121681738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.327A>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ANXA5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296511
Start	121686309:121686309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370872365
CDS Mutation	c.73C>T
AA Mutation	p.Arg25Trp(p.R25W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript