Colon Cancer: Gene >> FLT3LG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000594009
Start	49480352:49480352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.536C>A
AA Mutation	p.Pro179Gln(p.P179Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000594009
Start	49475781:49475781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.124G>A
AA Mutation	p.Ala42Thr(p.A42T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000594009
Start	49480383:49480383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.567A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000594009
Start	49478909:49478909(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs774922225
CDS Mutation	c.351delC
AA Mutation	p.Ser118AlafsTer24(p.S118Afs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FLT3LG

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000594009
Start	49475780:49475780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778371063
CDS Mutation	c.123C>T
Mutation Classification	Silent
Feature Type	Transcript