Colon Cancer: Gene >> HOXC4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303406
Start	54054958:54054958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.548G>A
AA Mutation	p.Arg183Gln(p.R183Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303406
Start	54055033:54055033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.623G>A
AA Mutation	p.Arg208His(p.R208H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000303406
Start	54054883:54054883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.473G>A
AA Mutation	p.Arg158His(p.R158H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303406
Start	54053994:54053994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.72G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303406
Start	54054156:54054156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.234G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303406
Start	54054866:54054866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.456C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303406
Start	54054340:54054340(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs764453660
CDS Mutation	c.424delA
AA Mutation	p.Ile142PhefsTer6(p.I142Ffs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HOXC4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303406
Start	54054022:54054022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.100C>A
AA Mutation	p.Pro34Thr(p.P34T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript