Colon Cancer: Gene >> NRG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361474
Start	139852944:139852944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1376G>A
AA Mutation	p.Ser459Asn(p.S459N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361474
Start	139887374:139887374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.838A>G
AA Mutation	p.Ser280Gly(p.S280G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361474
Start	139880874:139880874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774237401
CDS Mutation	c.973C>T
AA Mutation	p.Arg325Trp(p.R325W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361474
Start	139887475:139887475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749464757
CDS Mutation	c.737C>T
AA Mutation	p.Thr246Met(p.T246M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361474
Start	139851723:139851723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1653A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361474
Start	139880875:139880875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.972C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361474
Start	139871762:139871762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1071C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361474
Start	139871810:139871810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151296995
CDS Mutation	c.1023C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000361474
Start	140042622:140042622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.448C>T
AA Mutation	p.Arg150Ter(p.R150*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NRG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361474
Start	139865610:139865610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1128C>A
AA Mutation	p.Phe376Leu(p.F376L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361474
Start	139865606:139865606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1132G>A
AA Mutation	p.Gly378Arg(p.G378R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361474
Start	139851701:139851701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148371256
CDS Mutation	c.1675C>T
AA Mutation	p.Arg559Trp(p.R559W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript