Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> GSG1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000447459
Start	27884510:27884510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762645029
CDS Mutation	c.526G>A
AA Mutation	p.Ala176Thr(p.A176T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000447459
Start	27845019:27845019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.593T>C
AA Mutation	p.Phe198Ser(p.F198S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447459
Start	27828869:27828869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.750C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447459
Start	27884616:27884616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.420C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447459
Start	27884598:27884598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.438T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GSG1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000447459
Start	27963192:27963192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.361C>T
AA Mutation	p.Arg121Cys(p.R121C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000447459
Start	27884533:27884533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.503A>G
AA Mutation	p.Asp168Gly(p.D168G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447459
Start	27828893:27828893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.726C>A
Mutation Classification	Silent
Feature Type	Transcript