Colon Cancer: Gene >> HOXD13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392539
Start	176093449:176093449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774419506
CDS Mutation	c.559G>A
AA Mutation	p.Ala187Thr(p.A187T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392539
Start	176094504:176094504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.806A>G
AA Mutation	p.Asp269Gly(p.D269G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392539
Start	176094519:176094519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770519205
CDS Mutation	c.821G>A
AA Mutation	p.Arg274Gln(p.R274Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392539
Start	176093614:176093614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.724G>A
AA Mutation	p.Val242Met(p.V242M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000392539
Start	176094582:176094582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.884A>G
AA Mutation	p.Tyr295Cys(p.Y295C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HOXD13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392539
Start	176094597:176094597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.899T>C
AA Mutation	p.Phe300Ser(p.F300S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript