Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> HOXD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331462
Start	176189928:176189928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.773G>A
AA Mutation	p.Arg258Gln(p.R258Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331462
Start	176189255:176189255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.454G>A
AA Mutation	p.Val152Met(p.V152M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331462
Start	176189997:176189997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.842G>T
AA Mutation	p.Arg281Met(p.R281M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331462
Start	176189847:176189847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751102076
CDS Mutation	c.692C>T
AA Mutation	p.Ala231Val(p.A231V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000331462
Start	176190138:176190138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.983C>T
AA Mutation	p.Ser328Leu(p.S328L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331462
Start	176189293:176189293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766880295
CDS Mutation	c.492G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HOXD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331462
Start	176189967:176189967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.812C>T
AA Mutation	p.Thr271Met(p.T271M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331462
Start	176190111:176190111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.956G>A
AA Mutation	p.Gly319Asp(p.G319D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000331462
Start	176189894:176189894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.739G>T
AA Mutation	p.Glu247Ter(p.E247*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript