Colon Cancer: Gene >> MEF2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000424583
Start	19147805:19147805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138148108
CDS Mutation	c.286G>A
AA Mutation	p.Asp96Asn(p.D96N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000424583
Start	19147824:19147824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.267G>T
AA Mutation	p.Lys89Asn(p.K89N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000424583
Start	19147133:19147133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755456384
CDS Mutation	c.444G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000424583
Start	19146814:19146814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.603C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000424583
Start	19146601:19146601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142032500
CDS Mutation	c.723C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000424583
Start	19149406:19149406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757194042
CDS Mutation	c.78C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000424583
Start	19150712:19150712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.24C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000424583
Start	19146335:19146335(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.819delC
AA Mutation	p.Thr274ProfsTer130(p.T274Pfs*130)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000424583
Start	19146557:19146557(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.767delC
AA Mutation	p.Pro256GlnfsTer148(p.P256Qfs*148)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MEF2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000424583
Start	19150719:19150719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.17T>C
AA Mutation	p.Ile6Thr(p.I6T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript