Colon Cancer: Gene >> ANXA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257497
Start	73162841:73162841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533499971
CDS Mutation	c.535G>A
AA Mutation	p.Ala179Thr(p.A179T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000257497
Start	73169060:73169060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.890T>C
AA Mutation	p.Ile297Thr(p.I297T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000257497
Start	73169071:73169071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.901G>A
AA Mutation	p.Val301Ile(p.V301I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000257497
Start	73163524:73163524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.604G>A
AA Mutation	p.Asp202Asn(p.D202N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000257497
Start	73167525:73167525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.831C>A
AA Mutation	p.Phe277Leu(p.F277L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000257497
Start	73169051:73169051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.881A>G
AA Mutation	p.Lys294Arg(p.K294R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257497
Start	73158766:73158766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148187721
CDS Mutation	c.138G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ANXA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257497
Start	73162805:73162805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.499G>T
AA Mutation	p.Asp167Tyr(p.D167Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000257497
Start	73160363:73160363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752285742
CDS Mutation	c.371G>A
AA Mutation	p.Arg124His(p.R124H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000257497
Start	73160849:73160849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.431G>T
AA Mutation	p.Arg144Ile(p.R144I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000257497
Start	73163483:73163483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.563G>A
AA Mutation	p.Arg188Gln(p.R188Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript