Colon Cancer: Gene >> HSF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000528838
Start	144309490:144309490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782798876
CDS Mutation	c.262G>A
AA Mutation	p.Gly88Ser(p.G88S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000528838
Start	144314149:144314149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782078876
CDS Mutation	c.1409C>T
AA Mutation	p.Ala470Val(p.A470V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000528838
Start	144309485:144309485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.257A>G
AA Mutation	p.Gln86Arg(p.Q86R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000528838
Start	144308982:144308982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.194A>G
AA Mutation	p.Asn65Ser(p.N65S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000528838
Start	144311364:144311364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.608T>C
AA Mutation	p.Leu203Pro(p.L203P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000528838
Start	144309806:144309806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148595793
CDS Mutation	c.398G>A
AA Mutation	p.Arg133His(p.R133H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000528838
Start	144314180:144314180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1440C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000528838
Start	144312190:144312190(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs782124112
CDS Mutation	c.1094delC
AA Mutation	p.Pro365ArgfsTer12(p.P365Rfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HSF1

No Mutation Annotation!