Colon Cancer: Gene >> CLEC10A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000254868
Start	7078083:7078083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200835319
CDS Mutation	c.98G>A
AA Mutation	p.Arg33His(p.R33H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000254868
Start	7078802:7078802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368746225
CDS Mutation	c.11C>T
AA Mutation	p.Thr4Met(p.T4M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000254868
Start	7076949:7076949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.223G>T
AA Mutation	p.Asp75Tyr(p.D75Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000254868
Start	7078077:7078077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.104G>A
AA Mutation	p.Cys35Tyr(p.C35Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000254868
Start	7075448:7075448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.694C>A
AA Mutation	p.Leu232Ile(p.L232I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000254868
Start	7076041:7076041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.464A>C
AA Mutation	p.Gln155Pro(p.Q155P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000254868
Start	7075835:7075835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.571A>C
AA Mutation	p.Ser191Arg(p.S191R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254868
Start	7075093:7075093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147465833
CDS Mutation	c.912C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000254868
Start	7076968:7076968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.204C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000254868
Start	7075886:7075886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.521-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CLEC10A

No Mutation Annotation!