Colon Cancer: Gene >> FOXD4L4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377413
Start	65737206:65737206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.61G>A
AA Mutation	p.Asp21Asn(p.D21N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377413
Start	65737257:65737257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.112G>A
AA Mutation	p.Glu38Lys(p.E38K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377413
Start	65738388:65738388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1243C>T
AA Mutation	p.Arg415Cys(p.R415C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377413
Start	65737359:65737359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.214G>A
AA Mutation	p.Glu72Lys(p.E72K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377413
Start	65737552:65737552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.407C>T
AA Mutation	p.Ala136Val(p.A136V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377413
Start	65738071:65738071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.926G>A
AA Mutation	p.Arg309Lys(p.R309K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000377413
Start	65737752:65737752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.607C>T
AA Mutation	p.Arg203Cys(p.R203C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000377413
Start	65738190:65738190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1045C>T
AA Mutation	p.Arg349Cys(p.R349C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377413
Start	65737349:65737349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.204G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377413
Start	65738036:65738036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.891G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377413
Start	65737184:65737184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.39G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377413
Start	65737256:65737256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.111C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FOXD4L4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377413
Start	65737315:65737315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.170C>T
AA Mutation	p.Pro57Leu(p.P57L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377413
Start	65737197:65737197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.52C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000377413
Start	65737337:65737337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.192G>A
AA Mutation	p.Trp64Ter(p.W64*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript