Colon Cancer: Gene >> HOXD10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000249501
Start	176117207:176117207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.374C>T
AA Mutation	p.Ser125Leu(p.S125L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000249501
Start	176116894:176116894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765114168
CDS Mutation	c.61G>A
AA Mutation	p.Ala21Thr(p.A21T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000249501
Start	176116937:176116937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.104A>G
AA Mutation	p.Tyr35Cys(p.Y35C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000249501
Start	176117380:176117380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.547C>T
AA Mutation	p.Arg183Cys(p.R183C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249501
Start	176117307:176117307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.474C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249501
Start	176117385:176117385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756832722
CDS Mutation	c.552C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249501
Start	176116998:176116998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.165G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249501
Start	176117233:176117233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.400C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000249501
Start	176119202:176119202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.994G>T
AA Mutation	p.Glu332Ter(p.E332*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000249501
Start	176119160:176119160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.952C>T
AA Mutation	p.Arg318Ter(p.R318*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HOXD10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000249501
Start	176119221:176119221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761758159
CDS Mutation	c.1013C>T
AA Mutation	p.Thr338Met(p.T338M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000249501
Start	176117344:176117344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770037719
CDS Mutation	c.511G>A
AA Mutation	p.Glu171Lys(p.E171K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000249501
Start	176117099:176117099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374700658
CDS Mutation	c.266G>A
AA Mutation	p.Arg89Gln(p.R89Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249501
Start	176117079:176117079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.246A>C
Mutation Classification	Silent
Feature Type	Transcript