Colon Cancer: Gene >> NAPA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263354
Start	47490826:47490826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.697C>T
AA Mutation	p.Pro233Ser(p.P233S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263354
Start	47500684:47500684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.244G>A
AA Mutation	p.Ala82Thr(p.A82T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263354
Start	47503474:47503474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.127G>A
AA Mutation	p.Glu43Lys(p.E43K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263354
Start	47503475:47503475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760072222
CDS Mutation	c.126C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263354
Start	47493133:47493133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.462C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000263354
Start	47514856:47514858(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs760353871
CDS Mutation	c.83_85delTCT
AA Mutation	p.Phe28del(p.F28del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NAPA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263354
Start	47503474:47503474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.127G>A
AA Mutation	p.Glu43Lys(p.E43K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263354
Start	47493446:47493446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.390C>A
Mutation Classification	Silent
Feature Type	Transcript