Colon Cancer: Gene >> ANXA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396024
Start	60364481:60364481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.191G>T
AA Mutation	p.Ser64Ile(p.S64I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396024
Start	60352401:60352401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374077954
CDS Mutation	c.664G>A
AA Mutation	p.Val222Met(p.V222M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000396024
Start	60364452:60364452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774410888
CDS Mutation	c.220G>A
AA Mutation	p.Ala74Thr(p.A74T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000396024
Start	60386060:60386060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.16G>A
AA Mutation	p.Glu6Lys(p.E6K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ANXA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396024
Start	60347686:60347686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.964G>C
AA Mutation	p.Asp322His(p.D322H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396024
Start	60355939:60355939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.508C>A
AA Mutation	p.Leu170Met(p.L170M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript