Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> NRAS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369535
Start	114716124:114716124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121434595
CDS Mutation	c.37G>C
AA Mutation	p.Gly13Arg(p.G13R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369535
Start	114713909:114713909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913254
CDS Mutation	c.181C>A
AA Mutation	p.Gln61Lys(p.Q61K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369535
Start	114713908:114713908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs11554290
CDS Mutation	c.182A>T
AA Mutation	p.Gln61Leu(p.Q61L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369535
Start	114713864:114713864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753954415
CDS Mutation	c.226G>A
AA Mutation	p.Glu76Lys(p.E76K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369535
Start	114716126:114716126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913237
CDS Mutation	c.35G>A
AA Mutation	p.Gly12Asp(p.G12D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369535
Start	114708615:114708615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.490C>T
AA Mutation	p.Arg164Cys(p.R164C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369535
Start	114716126:114716126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913237
CDS Mutation	c.35G>C
AA Mutation	p.Gly12Ala(p.G12A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000369535
Start	114713908:114713908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs11554290
CDS Mutation	c.182A>G
AA Mutation	p.Gln61Arg(p.Q61R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000369535
Start	114709625:114709625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.394G>A
AA Mutation	p.Glu132Lys(p.E132K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000369535
Start	114716127:114716127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913250
CDS Mutation	c.34G>T
AA Mutation	p.Gly12Cys(p.G12C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000369535
Start	114716126:114716126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913237
CDS Mutation	c.35G>T
AA Mutation	p.Gly12Val(p.G12V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369535
Start	114716145:114716145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.16C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NRAS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369535
Start	114713909:114713909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913254
CDS Mutation	c.181C>A
AA Mutation	p.Gln61Lys(p.Q61K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369535
Start	114716126:114716126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913237
CDS Mutation	c.35G>A
AA Mutation	p.Gly12Asp(p.G12D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369535
Start	114713907:114713907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.183A>C
AA Mutation	p.Gln61His(p.Q61H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369535
Start	114716127:114716127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121913250
CDS Mutation	c.34G>T
AA Mutation	p.Gly12Cys(p.G12C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369535
Start	114716123:114716123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121434596
CDS Mutation	c.38G>A
AA Mutation	p.Gly13Asp(p.G13D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369535
Start	114716124:114716124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121434595
CDS Mutation	c.37G>C
AA Mutation	p.Gly13Arg(p.G13R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369535
Start	114713908:114713908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs11554290
CDS Mutation	c.182A>G
AA Mutation	p.Gln61Arg(p.Q61R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript