Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CORO2A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343933
Start	98126599:98126599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1396A>G
AA Mutation	p.Thr466Ala(p.T466A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343933
Start	98157541:98157541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.120C>A
AA Mutation	p.Phe40Leu(p.F40L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000343933
Start	98132191:98132191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.759G>T
AA Mutation	p.Trp253Cys(p.W253C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000343933
Start	98128696:98128696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.991G>A
AA Mutation	p.Asp331Asn(p.D331N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000343933
Start	98137652:98137652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs2231658
CDS Mutation	c.238G>A
AA Mutation	p.Gly80Arg(p.G80R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343933
Start	98134878:98134878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147316581
CDS Mutation	c.396G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CORO2A

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343933
Start	98133106:98133106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.580C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343933
Start	98128676:98128676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1011C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343933
Start	98126579:98126579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267602332
CDS Mutation	c.1416C>T
Mutation Classification	Silent
Feature Type	Transcript