Colon Cancer: Gene >> MEF2A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354410
Start	99710682:99710682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748043464
CDS Mutation	c.1040C>T
AA Mutation	p.Ser347Leu(p.S347L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354410
Start	99671524:99671524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.263T>C
AA Mutation	p.Leu88Pro(p.L88P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354410
Start	99645567:99645567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.61T>G
AA Mutation	p.Phe21Val(p.F21V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000354410
Start	99710664:99710664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1022C>T
AA Mutation	p.Ala341Val(p.A341V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000354410
Start	99674601:99674601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.605C>A
AA Mutation	p.Thr202Asn(p.T202N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000354410
Start	99645575:99645575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.69G>T
AA Mutation	p.Lys23Asn(p.K23N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000354410
Start	99645618:99645618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.112C>T
AA Mutation	p.Leu38Phe(p.L38F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354410
Start	99712543:99712543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541112324
CDS Mutation	c.1272G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354410
Start	99675412:99675412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.630C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354410
Start	99645641:99645641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.135C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354410
Start	99645666:99645666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.160C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000354410
Start	99712700:99712700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1429C>T
AA Mutation	p.Arg477Ter(p.R477*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000354410
Start	99645664:99645665(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.158_159insTAAAAAAGGTAT
AA Mutation	p.Lys53delinsAsnLysLysGlyIle(p.K53delinsNKKGI)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MEF2A

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000354410
Start	99690384:99690384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.820C>T
AA Mutation	p.Arg274Ter(p.R274*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript