Colon Cancer: Gene >> HSPA9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297185
Start	138557465:138557465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1665A>C
AA Mutation	p.Lys555Asn(p.K555N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297185
Start	138567470:138567470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.701A>C
AA Mutation	p.Lys234Thr(p.K234T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000297185
Start	138559986:138559986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1288G>A
AA Mutation	p.Gly430Ser(p.G430S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000297185
Start	138561588:138561588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1174A>G
AA Mutation	p.Met392Val(p.M392V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000297185
Start	138567030:138567030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776644009
CDS Mutation	c.850C>T
AA Mutation	p.Arg284Trp(p.R284W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000297185
Start	138556108:138556108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1969T>C
AA Mutation	p.Ser657Pro(p.S657P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297185
Start	138567715:138567715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.543C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297185
Start	138559968:138559968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1306C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297185
Start	138575250:138575250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.69C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297185
Start	138561640:138561640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1122A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000297185
Start	138561618:138561618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1144G>T
AA Mutation	p.Glu382Ter(p.E382*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HSPA9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297185
Start	138557409:138557409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372075340
CDS Mutation	c.1721G>A
AA Mutation	p.Arg574Gln(p.R574Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297185
Start	138559869:138559869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1405A>G
AA Mutation	p.Ser469Gly(p.S469G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297185
Start	138571046:138571046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754498058
CDS Mutation	c.324G>A
Mutation Classification	Silent
Feature Type	Transcript