Mutation

Primary Site >> Stomach Cancer

Gene >> BMP4

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000245451
Start	53950384:53950384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768059149
CDS Mutation	c.875G>A
AA Mutation	p.Arg292His(p.R292H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000245451
Start	53952021:53952021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.202C>T
AA Mutation	p.Arg68Cys(p.R68C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000245451
Start	53950883:53950883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.376C>G
AA Mutation	p.Leu126Val(p.L126V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000245451
Start	53952017:53952017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.206G>A
AA Mutation	p.Arg69His(p.R69H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000245451
Start	53952158:53952158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.65G>A
AA Mutation	p.Ser22Asn(p.S22N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000245451
Start	53952059:53952059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755084602
CDS Mutation	c.164G>A
AA Mutation	p.Arg55Gln(p.R55Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000245451
Start	53952215:53952215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8C>A
AA Mutation	p.Pro3His(p.P3H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000245451
Start	53950628:53950628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748940819
CDS Mutation	c.631C>T
AA Mutation	p.Arg211Trp(p.R211W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000245451
Start	53950081:53950081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1178T>C
AA Mutation	p.Val393Ala(p.V393A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245451
Start	53952088:53952088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.135C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245451
Start	53950737:53950737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.522C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245451
Start	53950560:53950560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.699G>A
Mutation Classification	Silent
Feature Type	Transcript