Colon Cancer: Gene >> UVRAG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356136
Start	75851920:75851920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.155A>G
AA Mutation	p.Asn52Ser(p.N52S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356136
Start	75879900:75879900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.292G>A
AA Mutation	p.Asp98Asn(p.D98N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356136
Start	75851893:75851893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.128G>A
AA Mutation	p.Arg43Gln(p.R43Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356136
Start	75888839:75888839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370425154
CDS Mutation	c.443G>A
AA Mutation	p.Arg148Gln(p.R148Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356136
Start	76016908:76016908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1154C>A
AA Mutation	p.Pro385His(p.P385H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356136
Start	76008812:76008812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1005A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356136
Start	76008836:76008836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1029T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000356136
Start	75983387:75983387(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs770844823
CDS Mutation	c.709delA
AA Mutation	p.Ser237ValfsTer6(p.S237Vfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> UVRAG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356136
Start	75879900:75879900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.292G>A
AA Mutation	p.Asp98Asn(p.D98N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356136
Start	76141242:76141242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1929C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000356136
Start	75852000:75852000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.235G>T
AA Mutation	p.Glu79Ter(p.E79*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript