Colon Cancer: Gene >> VSIG4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374737
Start	66022857:66022857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.946G>A
AA Mutation	p.Val316Ile(p.V316I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374737
Start	66033559:66033559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.327C>A
AA Mutation	p.Ser109Arg(p.S109R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374737
Start	66025043:66025043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750631892
CDS Mutation	c.922C>T
AA Mutation	p.Arg308Trp(p.R308W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374737
Start	66032547:66032547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.615C>G
AA Mutation	p.Asp205Glu(p.D205E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374737
Start	66028069:66028069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.738C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374737
Start	66022269:66022269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1194C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> VSIG4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374737
Start	66022851:66022851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752906800
CDS Mutation	c.952G>A
AA Mutation	p.Glu318Lys(p.E318K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript