Colon Cancer: Gene >> MBNL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282486
Start	152432823:152432823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.452C>A
AA Mutation	p.Pro151Gln(p.P151Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282486
Start	152300234:152300234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.41T>C
AA Mutation	p.Leu14Pro(p.L14P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282486
Start	152415017:152415017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.251G>A
AA Mutation	p.Arg84His(p.R84H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000282486
Start	152414951:152414951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.185C>T
AA Mutation	p.Ser62Phe(p.S62F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000282486
Start	152445481:152445481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.749C>T
AA Mutation	p.Ala250Val(p.A250V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282486
Start	152414997:152414997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199543138
CDS Mutation	c.231G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282486
Start	152432878:152432878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.507T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000282486
Start	152445504:152445527(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.780_803delACAGGCTGCAGCCACCGCAGCTGC
AA Mutation	p.Gln261_Ala268del(p.Q261_A268del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MBNL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282486
Start	152300347:152300347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.154G>A
AA Mutation	p.Ala52Thr(p.A52T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282486
Start	152445485:152445485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.753A>G
Mutation Classification	Silent
Feature Type	Transcript