Colon Cancer: Gene >> PRKAR2A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265563
Start	48773071:48773071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.580A>G
AA Mutation	p.Thr194Ala(p.T194A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265563
Start	48847383:48847383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.214G>A
AA Mutation	p.Ala72Thr(p.A72T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265563
Start	48751699:48751699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150452598
CDS Mutation	c.1101C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265563
Start	48765049:48765049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.828A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PRKAR2A

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000265563
Start	48782987:48782987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201062271
CDS Mutation	c.541C>T
AA Mutation	p.Arg181Trp(p.R181W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265563
Start	48765068:48765068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776689351
CDS Mutation	c.809G>A
AA Mutation	p.Arg270Gln(p.R270Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript