Mutation

Primary Site >> Stomach Cancer

Gene >> MBD3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000434436
Start	1581137:1581137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757544695
CDS Mutation	c.632C>T
AA Mutation	p.Thr211Met(p.T211M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000434436
Start	1592582:1592582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.50G>T
AA Mutation	p.Arg17Met(p.R17M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000434436
Start	1585095:1585095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.230G>A
AA Mutation	p.Ser77Asn(p.S77N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000434436
Start	1581147:1581147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.622C>T
AA Mutation	p.Leu208Phe(p.L208F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000434436
Start	1584658:1584658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.290C>T
AA Mutation	p.Thr97Met(p.T97M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000434436
Start	1584559:1584559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.389C>T
AA Mutation	p.Ala130Val(p.A130V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000434436
Start	1581218:1581218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.551C>T
AA Mutation	p.Ala184Val(p.A184V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000434436
Start	1578405:1578405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532173134
CDS Mutation	c.811G>A
AA Mutation	p.Asp271Asn(p.D271N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000434436
Start	1584656:1584656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.292G>A
AA Mutation	p.Ala98Thr(p.A98T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000434436
Start	1578417:1578417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.799G>T
AA Mutation	p.Ala267Ser(p.A267S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000434436
Start	1581157:1581157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199983089
CDS Mutation	c.612C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000434436
Start	1578343:1578343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.873C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000434436
Start	1584647:1584647(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.301delG
AA Mutation	p.Val101CysfsTer12(p.V101Cfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000434436
Start	1592613:1592613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.19G>T
AA Mutation	p.Glu7Ter(p.E7*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript