Colon Cancer: Gene >> UPP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331803
Start	48106959:48106959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770919651
CDS Mutation	c.523C>T
AA Mutation	p.Arg175Trp(p.R175W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331803
Start	48101951:48101951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.290T>C
AA Mutation	p.Met97Thr(p.M97T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331803
Start	48108247:48108247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769939785
CDS Mutation	c.823C>T
AA Mutation	p.Arg275Cys(p.R275C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331803
Start	48103309:48103309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.334A>C
AA Mutation	p.Ile112Leu(p.I112L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000331803
Start	48107405:48107405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.691G>A
AA Mutation	p.Asp231Asn(p.D231N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331803
Start	48107030:48107030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755794187
CDS Mutation	c.594C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000331803
Start	48099705:48099706(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.85dupA
AA Mutation	p.Met29AsnfsTer14(p.M29Nfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> UPP1

No Mutation Annotation!