Colon Cancer: Gene >> PRKAR2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265717
Start	107159514:107159514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs76105568
CDS Mutation	c.1189G>A
AA Mutation	p.Ala397Thr(p.A397T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265717
Start	107156991:107156991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201018627
CDS Mutation	c.926C>T
AA Mutation	p.Ser309Leu(p.S309L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265717
Start	107146383:107146383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200774998
CDS Mutation	c.663C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265717
Start	107157236:107157236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1035G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000265717
Start	107157228:107157228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1027C>T
AA Mutation	p.Arg343Ter(p.R343*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PRKAR2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265717
Start	107070308:107070308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.335G>A
AA Mutation	p.Arg112His(p.R112H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265717
Start	107140886:107140886(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.521delT
AA Mutation	p.Leu174TrpfsTer8(p.L174Wfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript