Colon Cancer: Gene >> GNL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000418458
Start	52686813:52686813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.58A>C
AA Mutation	p.Lys20Gln(p.K20Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000418458
Start	52690953:52690953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.663G>T
AA Mutation	p.Lys221Asn(p.K221N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000418458
Start	52689078:52689078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.413T>G
AA Mutation	p.Ile138Ser(p.I138S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000418458
Start	52693234:52693234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1092T>G
AA Mutation	p.Phe364Leu(p.F364L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000418458
Start	52689201:52689201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.536A>C
AA Mutation	p.Lys179Thr(p.K179T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000418458
Start	52690605:52690605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.555G>T
AA Mutation	p.Lys185Asn(p.K185N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418458
Start	52690608:52690608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.558G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000418458
Start	52692969:52692969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745733070
CDS Mutation	c.967C>T
AA Mutation	p.Arg323Ter(p.R323*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GNL3

No Mutation Annotation!