Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CHML

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366553
Start	241635039:241635039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.728T>C
AA Mutation	p.Leu243Ser(p.L243S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366553
Start	241634560:241634560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762564140
CDS Mutation	c.1207C>T
AA Mutation	p.Arg403Cys(p.R403C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366553
Start	241634793:241634793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.974A>G
AA Mutation	p.Tyr325Cys(p.Y325C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366553
Start	241635471:241635471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.296C>G
AA Mutation	p.Thr99Arg(p.T99R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000366553
Start	241635072:241635072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.695A>T
AA Mutation	p.Asp232Val(p.D232V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366553
Start	241634534:241634534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368941629
CDS Mutation	c.1233C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366553
Start	241634231:241634231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1536T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366553
Start	241634246:241634246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532237518
CDS Mutation	c.1521G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366553
Start	241634777:241634777(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.990delA
AA Mutation	p.Lys330AsnfsTer2(p.K330Nfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CHML

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366553
Start	241634775:241634775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.992T>A
AA Mutation	p.Leu331Gln(p.L331Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366553
Start	241634466:241634466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1301T>G
AA Mutation	p.Phe434Cys(p.F434C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366553
Start	241635471:241635471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.296C>G
AA Mutation	p.Thr99Arg(p.T99R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366553
Start	241634560:241634560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762564140
CDS Mutation	c.1207C>T
AA Mutation	p.Arg403Cys(p.R403C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366553
Start	241634338:241634338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1429C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366553
Start	241634849:241634849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.918G>A
Mutation Classification	Silent
Feature Type	Transcript