Colon Cancer: Gene >> POU2F3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000543440
Start	120246475:120246475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201020292
CDS Mutation	c.55G>A
AA Mutation	p.Asp19Asn(p.D19N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000543440
Start	120302301:120302301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.377T>C
AA Mutation	p.Leu126Pro(p.L126P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000543440
Start	120305682:120305682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772841579
CDS Mutation	c.666C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000543440
Start	120298381:120298381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.249C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> POU2F3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000543440
Start	120307574:120307574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373394231
CDS Mutation	c.865G>A
AA Mutation	p.Glu289Lys(p.E289K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000543440
Start	120269218:120269218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.106C>T
AA Mutation	p.Arg36Ter(p.R36*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript