Colon Cancer: Gene >> NOMO2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381474
Start	18527614:18527614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1817A>G
AA Mutation	p.Gln606Arg(p.Q606R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381474
Start	18520798:18520798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141824052
CDS Mutation	c.2240G>A
AA Mutation	p.Gly747Asp(p.G747D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381474
Start	18538910:18538910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531974952
CDS Mutation	c.1018G>A
AA Mutation	p.Glu340Lys(p.E340K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381474
Start	18561918:18561918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.123C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381474
Start	18542684:18542684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.783A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381474
Start	18542633:18542633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.834G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000381474
Start	18531139:18531139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1567C>T
AA Mutation	p.Gln523Ter(p.Q523*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000381474
Start	18538655:18538655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1091C>A
AA Mutation	p.Ser364Ter(p.S364*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NOMO2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381474
Start	18520779:18520779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2259C>A
AA Mutation	p.Phe753Leu(p.F753L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381474
Start	18538649:18538649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766525830
CDS Mutation	c.1097G>A
AA Mutation	p.Arg366His(p.R366H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript