Colon Cancer: Gene >> MBNL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376673
Start	97276332:97276332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.97G>A
AA Mutation	p.Glu33Lys(p.E33K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376673
Start	97391427:97391427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1100A>T
AA Mutation	p.Glu367Val(p.E367V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376673
Start	97346923:97346923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.660T>A
AA Mutation	p.Asp220Glu(p.D220E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376673
Start	97357569:97357569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.892G>A
AA Mutation	p.Val298Ile(p.V298I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376673
Start	97391403:97391403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1076A>G
AA Mutation	p.Tyr359Cys(p.Y359C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000376673
Start	97347027:97347027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148388439
CDS Mutation	c.764C>T
AA Mutation	p.Ala255Val(p.A255V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000376673
Start	97346987:97346987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.724G>A
AA Mutation	p.Ala242Thr(p.A242T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376673
Start	97346935:97346935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.672G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376673
Start	97391347:97391347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750533362
CDS Mutation	c.1020C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376673
Start	97334317:97334317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772319502
CDS Mutation	c.216G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MBNL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376673
Start	97391348:97391348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369342078
CDS Mutation	c.1021G>A
AA Mutation	p.Gly341Arg(p.G341R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376673
Start	97357517:97357517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.840G>T
AA Mutation	p.Lys280Asn(p.K280N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376673
Start	97343168:97343168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.492C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376673
Start	97347004:97347004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754842384
CDS Mutation	c.741G>A
Mutation Classification	Silent
Feature Type	Transcript