Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DONSON

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303071
Start	33584654:33584654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.721A>C
AA Mutation	p.Met241Leu(p.M241L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303071
Start	33581368:33581368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1284G>T
AA Mutation	p.Gln428His(p.Q428H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303071
Start	33581332:33581332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1320T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303071
Start	33584625:33584625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.750T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_retained_variant
Transcription ID	ENST00000303071
Start	33578308:33578308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1700G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303071
Start	33582230:33582230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.981G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000303071
Start	33586100:33586100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753740715
CDS Mutation	c.484C>T
AA Mutation	p.Arg162Ter(p.R162*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DONSON

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303071
Start	33582213:33582213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.998G>C
AA Mutation	p.Ser333Thr(p.S333T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303071
Start	33579559:33579559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751675539
CDS Mutation	c.1354C>T
AA Mutation	p.Arg452Trp(p.R452W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000303071
Start	33581964:33581964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1138C>A
AA Mutation	p.Leu380Ile(p.L380I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript