Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> HHEX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282728
Start	92690231:92690231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.245A>G
AA Mutation	p.His82Arg(p.H82R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282728
Start	92690182:92690182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.196C>T
AA Mutation	p.Arg66Trp(p.R66W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282728
Start	92694706:92694706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.751T>C
AA Mutation	p.Ser251Pro(p.S251P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282728
Start	92694666:92694666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs188232439
CDS Mutation	c.711G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282728
Start	92690190:92690190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.204G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HHEX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282728
Start	92694749:92694749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.794G>T
AA Mutation	p.Ser265Ile(p.S265I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282728
Start	92694747:92694747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.792A>C
AA Mutation	p.Lys264Asn(p.K264N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282728
Start	92692490:92692490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.484C>A
AA Mutation	p.Leu162Ile(p.L162I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript