Colon Cancer: Gene >> HNRNPU

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000283179
Start	244858194:244858194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1311A>C
AA Mutation	p.Glu437Asp(p.E437D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000283179
Start	244859338:244859338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1054A>C
AA Mutation	p.Lys352Gln(p.K352Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283179
Start	244862648:244862648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.774T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283179
Start	244858167:244858167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752673312
CDS Mutation	c.1338G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283179
Start	244864296:244864296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745379201
CDS Mutation	c.12G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000283179
Start	244855499:244855499(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2277delT
AA Mutation	p.Pro760LeufsTer74(p.P760Lfs*74)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HNRNPU

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000283179
Start	244857617:244857617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1595C>A
AA Mutation	p.Thr532Asn(p.T532N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283179
Start	244858218:244858218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754530060
CDS Mutation	c.1287C>T
Mutation Classification	Silent
Feature Type	Transcript