Colon Cancer: Gene >> HOXC13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000243056
Start	53945173:53945173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.910G>T
AA Mutation	p.Val304Leu(p.V304L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000243056
Start	53945107:53945107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.844A>C
AA Mutation	p.Ser282Arg(p.S282R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000243056
Start	53945093:53945093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.830A>C
AA Mutation	p.Lys277Thr(p.K277T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000243056
Start	53945053:53945053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.790C>T
AA Mutation	p.Arg264Cys(p.R264C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000243056
Start	53945131:53945131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.868C>T
AA Mutation	p.Arg290Cys(p.R290C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000243056
Start	53945100:53945100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747370796
CDS Mutation	c.837C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000243056
Start	53939422:53939422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.516C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000243056
Start	53939476:53939476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.570C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000243056
Start	53939237:53939237(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs760974507
CDS Mutation	c.336delC
AA Mutation	p.Thr113ProfsTer26(p.T113Pfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HOXC13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000243056
Start	53945234:53945234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201149022
CDS Mutation	c.971C>T
AA Mutation	p.Ala324Val(p.A324V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000243056
Start	53945127:53945127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.864G>T
AA Mutation	p.Glu288Asp(p.E288D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript