Colon Cancer: Gene >> CLEC11A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000250340
Start	50723611:50723611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.86G>T
AA Mutation	p.Trp29Leu(p.W29L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000250340
Start	50723992:50723992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.235G>A
AA Mutation	p.Glu79Lys(p.E79K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000250340
Start	50724079:50724079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.322G>T
AA Mutation	p.Val108Phe(p.V108F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000250340
Start	50723657:50723657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.132G>T
AA Mutation	p.Glu44Asp(p.E44D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250340
Start	50723552:50723552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.27T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250340
Start	50725407:50725407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.912C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250340
Start	50725213:50725213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755766827
CDS Mutation	c.718C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250340
Start	50724045:50724045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.288C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000250340
Start	50723939:50723939(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.187delG
AA Mutation	p.Asp63MetfsTer77(p.D63Mfs*77)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000250340
Start	50725079:50725079(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.585delA
AA Mutation	p.Ala196LeufsTer209(p.A196Lfs*209)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000250340
Start	50725443:50725443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.948C>A
AA Mutation	p.Tyr316Ter(p.Y316*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CLEC11A

No Mutation Annotation!