Colon Cancer: Gene >> CLEC4G

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328853
Start	7729466:7729466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547480428
CDS Mutation	c.782G>A
AA Mutation	p.Arg261His(p.R261H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328853
Start	7731760:7731760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.67C>T
AA Mutation	p.Arg23Cys(p.R23C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000328853
Start	7729502:7729502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.746A>T
AA Mutation	p.His249Leu(p.H249L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328853
Start	7730040:7730040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772662136
CDS Mutation	c.606C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CLEC4G

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328853
Start	7729373:7729373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.875A>T
AA Mutation	p.Asn292Ile(p.N292I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328853
Start	7729462:7729462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.786G>A
Mutation Classification	Silent
Feature Type	Transcript