Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> HEMGN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259456
Start	97931208:97931208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142085732
CDS Mutation	c.187C>T
AA Mutation	p.Arg63Cys(p.R63C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000259456
Start	97930670:97930670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.725T>G
AA Mutation	p.Leu242Arg(p.L242R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000259456
Start	97930313:97930313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1082C>A
AA Mutation	p.Pro361His(p.P361H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000259456
Start	97930404:97930404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.991G>A
AA Mutation	p.Glu331Lys(p.E331K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000259456
Start	97930758:97930758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.637G>T
AA Mutation	p.Asp213Tyr(p.D213Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259456
Start	97930135:97930135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1260A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259456
Start	97930981:97930981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.414A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000259456
Start	97927470:97927470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1369G>T
AA Mutation	p.Glu457Ter(p.E457*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HEMGN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259456
Start	97930818:97930818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.577G>A
AA Mutation	p.Asp193Asn(p.D193N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000259456
Start	97931177:97931177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779943930
CDS Mutation	c.218G>A
AA Mutation	p.Arg73Gln(p.R73Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000259456
Start	97930134:97930134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1261G>A
AA Mutation	p.Glu421Lys(p.E421K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000259456
Start	97930860:97930860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.535G>T
AA Mutation	p.Glu179Ter(p.E179*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000259456
Start	97930218:97930218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1177G>T
AA Mutation	p.Glu393Ter(p.E393*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000259456
Start	97927416:97927416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1423G>T
AA Mutation	p.Glu475Ter(p.E475*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000259456
Start	97931118:97931118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.277G>T
AA Mutation	p.Glu93Ter(p.E93*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript