Colon Cancer: Gene >> FOXP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376207
Start	49256847:49256847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140222626
CDS Mutation	c.551C>T
AA Mutation	p.Ser184Leu(p.S184L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376207
Start	49251441:49251441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs28935477
CDS Mutation	c.1189C>T
AA Mutation	p.Arg397Trp(p.R397W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376207
Start	49251371:49251371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1259G>T
AA Mutation	p.Arg420Met(p.R420M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376207
Start	49253941:49253941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.943A>G
AA Mutation	p.Ser315Gly(p.S315G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376207
Start	49251340:49251340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1290C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376207
Start	49258347:49258347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.159G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376207
Start	49254011:49254011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782371089
CDS Mutation	c.873C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376207
Start	49254005:49254005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.879A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FOXP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376207
Start	49253160:49253160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1010G>A
AA Mutation	p.Arg337Gln(p.R337Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376207
Start	49258378:49258378(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.128delG
AA Mutation	p.Gly43GlufsTer19(p.G43Efs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript