Colon Cancer: Gene >> NOP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322166
Start	6561712:6561712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1159C>T
AA Mutation	p.Arg387Trp(p.R387W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322166
Start	6563121:6563121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185687202
CDS Mutation	c.938G>A
AA Mutation	p.Arg313Gln(p.R313Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000322166
Start	6560496:6560496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1511C>T
AA Mutation	p.Ala504Val(p.A504V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000322166
Start	6563104:6563104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747540211
CDS Mutation	c.955A>C
AA Mutation	p.Thr319Pro(p.T319P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000322166
Start	6557444:6557444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1988C>T
AA Mutation	p.Thr663Ile(p.T663I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000322166
Start	6557204:6557204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2228A>G
AA Mutation	p.Lys743Arg(p.K743R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322166
Start	6563943:6563943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.478C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322166
Start	6561030:6561030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777701681
CDS Mutation	c.1248C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322166
Start	6561704:6561704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1167G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000322166
Start	6560224:6560224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1663C>T
AA Mutation	p.Arg555Ter(p.R555*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000322166
Start	6557021:6557022(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2410_2411insT
AA Mutation	p.Arg804MetfsTer13(p.R804Mfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NOP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322166
Start	6560948:6560948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1330G>A
AA Mutation	p.Gly444Arg(p.G444R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322166
Start	6563911:6563911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.510G>C
AA Mutation	p.Lys170Asn(p.K170N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322166
Start	6560513:6560513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1494T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000322166
Start	6563725:6563725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.577G>T
AA Mutation	p.Glu193Ter(p.E193*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript