Colon Cancer: Gene >> DLX4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000240306
Start	49973759:49973759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.539C>A
AA Mutation	p.Ser180Tyr(p.S180Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000240306
Start	49973927:49973927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202154782
CDS Mutation	c.707C>T
AA Mutation	p.Ser236Leu(p.S236L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000240306
Start	49969481:49969481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.13C>T
AA Mutation	p.Pro5Ser(p.P5S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000240306
Start	49973815:49973815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.595C>T
AA Mutation	p.Pro199Ser(p.P199S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000240306
Start	49969616:49969616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.148C>T
AA Mutation	p.Pro50Ser(p.P50S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000240306
Start	49973073:49973073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.284A>G
AA Mutation	p.Asp95Gly(p.D95G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000240306
Start	49973074:49973074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.285C>A
AA Mutation	p.Asp95Glu(p.D95E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000240306
Start	49973148:49973148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.359C>T
AA Mutation	p.Pro120Leu(p.P120L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000240306
Start	49973727:49973727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200916126
CDS Mutation	c.507C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000240306
Start	49969624:49969624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.156C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000240306
Start	49973124:49973124(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.339delC
AA Mutation	p.Ala114ProfsTer19(p.A114Pfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DLX4

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000240306
Start	49973823:49973823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.603C>A
Mutation Classification	Silent
Feature Type	Transcript