Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CLEC1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000298527
Start	9995198:9995198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753263519
CDS Mutation	c.487C>T
AA Mutation	p.Arg163Cys(p.R163C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000298527
Start	9997182:9997182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.261A>T
AA Mutation	p.Gln87His(p.Q87H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298527
Start	9998322:9998322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762074150
CDS Mutation	c.123C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298527
Start	9996990:9996990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.294A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000298527
Start	9993186:9993187(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.646_647insTAAAAATAACTCCA
AA Mutation	p.Cys216LeufsTer12(p.C216Lfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CLEC1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000298527
Start	9996964:9996964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.320G>T
AA Mutation	p.Arg107Ile(p.R107I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000298527
Start	9993259:9993259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.574A>C
AA Mutation	p.Asn192His(p.N192H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000298527
Start	9995216:9995216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.469C>T
AA Mutation	p.Arg157Cys(p.R157C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript