Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> G3BP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359707
Start	75657676:75657676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267600258
CDS Mutation	c.232C>T
AA Mutation	p.Arg78Cys(p.R78C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359707
Start	75645434:75645434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767685659
CDS Mutation	c.1445G>A
AA Mutation	p.Arg482His(p.R482H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359707
Start	75645614:75645614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1265A>G
AA Mutation	p.Asp422Gly(p.D422G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359707
Start	75647143:75647143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.943G>A
AA Mutation	p.Glu315Lys(p.E315K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000359707
Start	75645701:75645701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1178C>T
AA Mutation	p.Pro393Leu(p.P393L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359707
Start	75646354:75646354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1160G>A
AA Mutation	p.Arg387Lys(p.R387K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359707
Start	75645574:75645574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1305T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> G3BP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359707
Start	75645434:75645434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767685659
CDS Mutation	c.1445G>A
AA Mutation	p.Arg482His(p.R482H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359707
Start	75647110:75647110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.976C>T
AA Mutation	p.Arg326Cys(p.R326C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359707
Start	75656995:75656995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.371T>G
AA Mutation	p.Phe124Cys(p.F124C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript