Colon Cancer: Gene >> MEF2D

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000348159
Start	156468237:156468237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1310G>A
AA Mutation	p.Ser437Asn(p.S437N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000348159
Start	156477049:156477049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.818T>C
AA Mutation	p.Ile273Thr(p.I273T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000348159
Start	156477104:156477104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.763C>T
AA Mutation	p.Pro255Ser(p.P255S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000348159
Start	156479765:156479765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.428C>T
AA Mutation	p.Pro143Leu(p.P143L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348159
Start	156482572:156482572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756430794
CDS Mutation	c.123C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348159
Start	156479785:156479785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.408G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348159
Start	156477063:156477063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.804C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348159
Start	156480858:156480858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771689492
CDS Mutation	c.372C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000348159
Start	156479648:156479649(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.544dupC
AA Mutation	p.Gln182ProfsTer20(p.Q182Pfs*20)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MEF2D

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000348159
Start	156479612:156479612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.581G>T
AA Mutation	p.Gly194Val(p.G194V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000348159
Start	156482514:156482514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763802424
CDS Mutation	c.181G>A
AA Mutation	p.Asp61Asn(p.D61N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000348159
Start	156482560:156482560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.135C>G
Mutation Classification	Silent
Feature Type	Transcript