Colon Cancer: Gene >> MBD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269468
Start	50275707:50275707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771787035
CDS Mutation	c.685C>T
AA Mutation	p.Arg229Trp(p.R229W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269468
Start	50273410:50273410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1508C>T
AA Mutation	p.Ala503Val(p.A503V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000269468
Start	50275635:50275635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.757C>T
AA Mutation	p.Arg253Cys(p.R253C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000269468
Start	50274295:50274295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1037G>A
AA Mutation	p.Arg346Gln(p.R346Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000269468
Start	50273437:50273437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1481C>T
AA Mutation	p.Ala494Val(p.A494V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000269468
Start	50274209:50274209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1123C>T
AA Mutation	p.Arg375Cys(p.R375C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000269468
Start	50276398:50276398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.496C>T
AA Mutation	p.Arg166Trp(p.R166W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000269468
Start	50276397:50276397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.497G>A
AA Mutation	p.Arg166Gln(p.R166Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000269468
Start	50275650:50275650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.742C>T
AA Mutation	p.Arg248Cys(p.R248C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000269468
Start	50274326:50274326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1006C>T
AA Mutation	p.Arg336Cys(p.R336C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000269468
Start	50273707:50273707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1303A>G
AA Mutation	p.Thr435Ala(p.T435A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000269468
Start	50277128:50277128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.187G>A
AA Mutation	p.Asp63Asn(p.D63N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000269468
Start	50275027:50275027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.928C>T
AA Mutation	p.Pro310Ser(p.P310S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269468
Start	50274312:50274312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1020C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000269468
Start	50276713:50276714(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.423_424delAG
AA Mutation	p.Asp143TrpfsTer29(p.D143Wfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MBD1

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000269468
Start	50275614:50275614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.778C>T
AA Mutation	p.Arg260Ter(p.R260*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript