Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CORO1C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261401
Start	108647446:108647446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1382G>A
AA Mutation	p.Arg461His(p.R461H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261401
Start	108678387:108678387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.203G>A
AA Mutation	p.Arg68Gln(p.R68Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261401
Start	108658772:108658772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.596G>A
AA Mutation	p.Arg199Lys(p.R199K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261401
Start	108701170:108701170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.149T>C
AA Mutation	p.Ile50Thr(p.I50T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CORO1C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261401
Start	108652369:108652369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.904G>A
AA Mutation	p.Val302Ile(p.V302I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261401
Start	108658866:108658866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.502A>C
AA Mutation	p.Asn168His(p.N168H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261401
Start	108648650:108648650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1260C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261401
Start	108648752:108648752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1158C>A
Mutation Classification	Silent
Feature Type	Transcript