Mutation

Primary Site >> Stomach Cancer

Gene >> BMP6

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000283147
Start	7862380:7862380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1086C>A
AA Mutation	p.Phe362Leu(p.F362L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000283147
Start	7727352:7727352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.397C>T
AA Mutation	p.Pro133Ser(p.P133S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000283147
Start	7727506:7727506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.551G>A
AA Mutation	p.Arg184His(p.R184H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000283147
Start	7727119:7727119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.164A>C
AA Mutation	p.Gln55Pro(p.Q55P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000283147
Start	7862402:7862402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144134653
CDS Mutation	c.1108G>A
AA Mutation	p.Val370Met(p.V370M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000283147
Start	7879101:7879101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1232C>T
AA Mutation	p.Ala411Val(p.A411V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000283147
Start	7727451:7727451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.496G>A
AA Mutation	p.Ala166Thr(p.A166T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000283147
Start	7845167:7845167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566660170
CDS Mutation	c.692G>A
AA Mutation	p.Arg231His(p.R231H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283147
Start	7727210:7727210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.255G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283147
Start	7861559:7861559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751916939
CDS Mutation	c.966G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283147
Start	7880238:7880238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774047873
CDS Mutation	c.1437G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283147
Start	7862407:7862407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748897782
CDS Mutation	c.1113C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283147
Start	7727585:7727585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.630C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283147
Start	7727549:7727549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.594C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000283147
Start	7727478:7727478(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.527delC
AA Mutation	p.Pro176ArgfsTer25(p.P176Rfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000283147
Start	7862314:7862314(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1024delC
AA Mutation	p.Arg342GlufsTer24(p.R342Efs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript