Colon Cancer: Gene >> MEF2C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000437473
Start	88722828:88722828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1198G>T
AA Mutation	p.Asp400Tyr(p.D400Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000437473
Start	88751880:88751880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777918857
CDS Mutation	c.566G>A
AA Mutation	p.Arg189Gln(p.R189Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000437473
Start	88728566:88728566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1027C>G
AA Mutation	p.His343Asp(p.H343D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000437473
Start	88752027:88752027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.419A>G
AA Mutation	p.Asn140Ser(p.N140S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000437473
Start	88731880:88731880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.659G>A
AA Mutation	p.Arg220Gln(p.R220Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000437473
Start	88804618:88804618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.238A>T
AA Mutation	p.Thr80Ser(p.T80S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000437473
Start	88722708:88722708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1318C>T
AA Mutation	p.Arg440Trp(p.R440W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000437473
Start	88804647:88804647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.209C>T
AA Mutation	p.Thr70Met(p.T70M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000437473
Start	88761265:88761265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.322G>T
AA Mutation	p.Gly108Cys(p.G108C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000437473
Start	88722771:88722771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1255T>C
AA Mutation	p.Ser419Pro(p.S419P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000437473
Start	88761240:88761240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.347A>C
AA Mutation	p.Lys116Thr(p.K116T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000437473
Start	88761279:88761279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755436703
CDS Mutation	c.308C>T
AA Mutation	p.Ala103Val(p.A103V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000437473
Start	88722875:88722875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1151C>G
AA Mutation	p.Ser384Cys(p.S384C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000437473
Start	88761278:88761278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567797470
CDS Mutation	c.309G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000437473
Start	88761224:88761224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186648089
CDS Mutation	c.363C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000437473
Start	88823774:88823775(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.14dupA
AA Mutation	p.Ile6AspfsTer9(p.I6Dfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MEF2C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000437473
Start	88722702:88722702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1324G>A
AA Mutation	p.Glu442Lys(p.E442K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000437473
Start	88751872:88751872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.574A>C
AA Mutation	p.Ser192Arg(p.S192R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript