Colon Cancer: Gene >> FOXD4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382500
Start	118098:118098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.22C>T
AA Mutation	p.Arg8Cys(p.R8C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000382500
Start	116972:116972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1148C>T
AA Mutation	p.Ala383Val(p.A383V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000382500
Start	117693:117693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.427C>T
AA Mutation	p.Arg143Cys(p.R143C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000382500
Start	117668:117668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.452G>A
AA Mutation	p.Ser151Asn(p.S151N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000382500
Start	117962:117962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751809498
CDS Mutation	c.158C>T
AA Mutation	p.Pro53Leu(p.P53L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382500
Start	117625:117625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760871989
CDS Mutation	c.495C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382500
Start	116920:116920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763686353
CDS Mutation	c.1200G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382500
Start	117853:117853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.267G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382500
Start	117019:117019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1101G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382500
Start	118009:118009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.111C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000382500
Start	117159:117160(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.960_961delTT
AA Mutation	p.Ala322IlefsTer160(p.A322Ifs*160)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000382500
Start	117574:117574(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.546delC
AA Mutation	p.Ala183ProfsTer141(p.A183Pfs*141)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FOXD4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382500
Start	117200:117200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.920C>T
AA Mutation	p.Ala307Val(p.A307V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382500
Start	117748:117748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.372C>T
Mutation Classification	Silent
Feature Type	Transcript