Colon Cancer: Gene >> CLEC4M

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327325
Start	7767550:7767550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375821664
CDS Mutation	c.971G>A
AA Mutation	p.Arg324His(p.R324H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327325
Start	7763459:7763459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.113G>A
AA Mutation	p.Gly38Asp(p.G38D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327325
Start	7766729:7766729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.858G>T
AA Mutation	p.Gln286His(p.Q286H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000327325
Start	7763466:7763466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.120G>T
AA Mutation	p.Lys40Asn(p.K40N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000327325
Start	7765760:7765760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.337T>G
AA Mutation	p.Tyr113Asp(p.Y113D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327325
Start	7766741:7766741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs78409055
CDS Mutation	c.870C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327325
Start	7765675:7765675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376354063
CDS Mutation	c.252C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327325
Start	7765684:7765684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144919911
CDS Mutation	c.261C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327325
Start	7768982:7768982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750026133
CDS Mutation	c.1194C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CLEC4M

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327325
Start	7768846:7768846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147246014
CDS Mutation	c.1058G>A
AA Mutation	p.Arg353Gln(p.R353Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327325
Start	7766173:7766173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.750C>A
Mutation Classification	Silent
Feature Type	Transcript