Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> HSPA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304858
Start	133076735:133076735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.745G>A
AA Mutation	p.Gly249Arg(p.G249R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304858
Start	133076705:133076705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.715G>A
AA Mutation	p.Val239Met(p.V239M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304858
Start	133086787:133086787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.914A>C
AA Mutation	p.Lys305Thr(p.K305T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000304858
Start	133089609:133089609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1292T>C
AA Mutation	p.Val431Ala(p.V431A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304858
Start	133097250:133097250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1893G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304858
Start	133089571:133089571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1254A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000304858
Start	133103911:133103911(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2209delA
AA Mutation	p.Ser737AlafsTer9(p.S737Afs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000304858
Start	133088499:133088499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1081G>T
AA Mutation	p.Glu361Ter(p.E361*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained;frameshift_variant;splice_region_variant
Transcription ID	ENST00000304858
Start	133065036:133065037(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.164_165insTATATTTTAAT
AA Mutation	p.Gln55HisfsTer4(p.Q55Hfs*4)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HSPA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304858
Start	133091262:133091262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770551334
CDS Mutation	c.1448G>A
AA Mutation	p.Arg483Gln(p.R483Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304858
Start	133088418:133088418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1000G>A
AA Mutation	p.Asp334Asn(p.D334N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304858
Start	133076812:133076812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.822G>T
AA Mutation	p.Lys274Asn(p.K274N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000304858
Start	133088485:133088485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1067A>C
AA Mutation	p.Lys356Thr(p.K356T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000304858
Start	133103967:133103967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771075745
CDS Mutation	c.2260A>G
AA Mutation	p.Lys754Glu(p.K754E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000304858
Start	133076792:133076792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199586152
CDS Mutation	c.802C>G
AA Mutation	p.Gln268Glu(p.Q268E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript