Colon Cancer: Gene >> HSPD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345042
Start	197494746:197494746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.517A>G
AA Mutation	p.Thr173Ala(p.T173A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000345042
Start	197494657:197494657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.606G>T
AA Mutation	p.Lys202Asn(p.K202N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000345042
Start	197489039:197489039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751104797
CDS Mutation	c.1178G>A
AA Mutation	p.Arg393Gln(p.R393Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000345042
Start	197493429:197493429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.764A>G
AA Mutation	p.Gln255Arg(p.Q255R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000345042
Start	197489109:197489109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768557320
CDS Mutation	c.1108C>T
AA Mutation	p.Arg370Cys(p.R370C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000345042
Start	197498734:197498734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.115T>G
AA Mutation	p.Leu39Val(p.L39V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345042
Start	197497261:197497261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.306C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345042
Start	197489056:197489056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1161G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345042
Start	197488385:197488385(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1322delG
AA Mutation	p.Gly441ValfsTer14(p.G441Vfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HSPD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345042
Start	197489157:197489157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1060G>A
AA Mutation	p.Asp354Asn(p.D354N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000345042
Start	197497297:197497297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.270C>A
AA Mutation	p.Tyr90Ter(p.Y90*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000345042
Start	197488371:197488371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1336C>T
AA Mutation	p.Arg446Ter(p.R446*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript