Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> HSPA14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378372
Start	14870636:14870636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769292701
CDS Mutation	c.1420C>T
AA Mutation	p.Arg474Cys(p.R474C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378372
Start	14848826:14848826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.307G>T
AA Mutation	p.Asp103Tyr(p.D103Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378372
Start	14854275:14854275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.885G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378372
Start	14867741:14867741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1212G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378372
Start	14848797:14848797(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.284delA
AA Mutation	p.Asn95MetfsTer8(p.N95Mfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000378372
Start	14867107:14867107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1018C>T
AA Mutation	p.Arg340Ter(p.R340*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HSPA14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378372
Start	14854138:14854138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.748G>A
AA Mutation	p.Asp250Asn(p.D250N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378372
Start	14848815:14848815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766422205
CDS Mutation	c.296G>A
AA Mutation	p.Arg99Gln(p.R99Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378372
Start	14854202:14854202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.812C>A
AA Mutation	p.Ser271Tyr(p.S271Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378372
Start	14852397:14852397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.600A>G
Mutation Classification	Silent
Feature Type	Transcript