Colon Cancer: Gene >> U2AF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308924
Start	55669102:55669102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.965G>A
AA Mutation	p.Gly322Asp(p.G322D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308924
Start	55669606:55669606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1207C>T
AA Mutation	p.Arg403Trp(p.R403W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308924
Start	55668749:55668749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.902G>A
AA Mutation	p.Gly301Asp(p.G301D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000308924
Start	55661152:55661152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.449G>A
AA Mutation	p.Arg150His(p.R150H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308924
Start	55668726:55668726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.879C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308924
Start	55669611:55669611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150014824
CDS Mutation	c.1212C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308924
Start	55662539:55662540(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs758316280
CDS Mutation	c.531dupG
AA Mutation	p.Leu178AlafsTer15(p.L178Afs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> U2AF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308924
Start	55674054:55674054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1414C>T
AA Mutation	p.Arg472Trp(p.R472W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308924
Start	55668723:55668723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.876G>T
AA Mutation	p.Lys292Asn(p.K292N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript