Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> HDAC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373548
Start	32327059:32327059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.476C>T
AA Mutation	p.Ala159Val(p.A159V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373548
Start	32330894:32330894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565534358
CDS Mutation	c.965C>T
AA Mutation	p.Thr322Met(p.T322M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373548
Start	32332174:32332174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1304C>T
AA Mutation	p.Ser435Phe(p.S435F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373548
Start	32327611:32327611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376335337
CDS Mutation	c.570G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373548
Start	32332200:32332200(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1333delA
AA Mutation	p.Thr445GlnfsTer49(p.T445Qfs*49)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000373548
Start	32332725:32332727(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs771427696
CDS Mutation	c.1402_1404delGAG
AA Mutation	p.Glu468del(p.E468del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HDAC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373548
Start	32302663:32302663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.92A>C
AA Mutation	p.Lys31Thr(p.K31T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373548
Start	32329095:32329095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.664T>G
AA Mutation	p.Tyr222Asp(p.Y222D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373548
Start	32331709:32331709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767557241
CDS Mutation	c.1122G>A
Mutation Classification	Silent
Feature Type	Transcript