Colon Cancer: Gene >> PAICS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264221
Start	56451977:56451977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.877A>G
AA Mutation	p.Ile293Val(p.I293V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264221
Start	56441713:56441713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773166026
CDS Mutation	c.67G>A
AA Mutation	p.Glu23Lys(p.E23K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264221
Start	56448538:56448538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.514A>G
AA Mutation	p.Ile172Val(p.I172V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264221
Start	56451982:56451982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.882A>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PAICS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264221
Start	56451948:56451948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.848A>C
AA Mutation	p.Lys283Thr(p.K283T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000264221
Start	56451992:56451992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772673782
CDS Mutation	c.892C>T
AA Mutation	p.Arg298Ter(p.R298*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript