Colon Cancer: Gene >> NMNAT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287713
Start	183284010:183284010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.559C>T
AA Mutation	p.Arg187Trp(p.R187W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287713
Start	183292841:183292841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.191G>A
AA Mutation	p.Arg64Gln(p.R64Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287713
Start	183261260:183261260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768849266
CDS Mutation	c.695G>A
AA Mutation	p.Arg232Gln(p.R232Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000287713
Start	183292835:183292835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200887683
CDS Mutation	c.197G>A
AA Mutation	p.Arg66His(p.R66H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000287713
Start	183284755:183284755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760875625
CDS Mutation	c.484C>T
AA Mutation	p.Arg162Trp(p.R162W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287713
Start	183418244:183418244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.24C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287713
Start	183284771:183284771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.468G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NMNAT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287713
Start	183286760:183286760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.350T>C
AA Mutation	p.Val117Ala(p.V117A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287713
Start	183293757:183293757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.122T>G
AA Mutation	p.Phe41Cys(p.F41C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287713
Start	183252722:183252722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150203304
CDS Mutation	c.843C>T
Mutation Classification	Silent
Feature Type	Transcript