Colon Cancer: Gene >> UBA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246548
Start	34469127:34469127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs575391206
CDS Mutation	c.1829G>A
AA Mutation	p.Arg610His(p.R610H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000246548
Start	34430610:34430610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.173A>G
AA Mutation	p.Asn58Ser(p.N58S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000246548
Start	34466895:34466895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1622A>T
AA Mutation	p.Asp541Val(p.D541V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000246548
Start	34434874:34434874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.365G>A
AA Mutation	p.Arg122Gln(p.R122Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246548
Start	34451991:34451991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146405147
CDS Mutation	c.882G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246548
Start	34452087:34452087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367637106
CDS Mutation	c.978C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246548
Start	34454517:34454517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1206A>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> UBA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246548
Start	34469073:34469073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369166559
CDS Mutation	c.1775C>T
AA Mutation	p.Ser592Leu(p.S592L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000246548
Start	34443899:34443899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.637C>T
AA Mutation	p.Pro213Ser(p.P213S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000246548
Start	34458769:34458770(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs766436639
CDS Mutation	c.1253dupT
AA Mutation	p.Leu418PhefsTer3(p.L418Ffs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript