Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> GOLGA6A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290438
Start	74071616:74071616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1634C>T
AA Mutation	p.Thr545Met(p.T545M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000290438
Start	74070917:74070917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2075A>G
AA Mutation	p.Asp692Gly(p.D692G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290438
Start	74080640:74080640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201579908
CDS Mutation	c.180C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290438
Start	74072224:74072224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1587G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000290438
Start	74070921:74070921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2071C>T
AA Mutation	p.Gln691Ter(p.Q691*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GOLGA6A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290438
Start	74075702:74075702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.740T>A
AA Mutation	p.Met247Lys(p.M247K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000290438
Start	74074756:74074756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1093G>A
AA Mutation	p.Glu365Lys(p.E365K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000290438
Start	74070948:74070948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2044C>A
AA Mutation	p.Gln682Lys(p.Q682K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000290438
Start	74080729:74080729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.91G>T
AA Mutation	p.Glu31Ter(p.E31*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript