Mutation

Primary Site >> Stomach Cancer

Gene >> BCR

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305877
Start	23288131:23288131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372445084
CDS Mutation	c.2561G>A
AA Mutation	p.Arg854His(p.R854H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000305877
Start	23260960:23260960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367931519
CDS Mutation	c.1472A>G
AA Mutation	p.Asp491Gly(p.D491G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000305877
Start	23181567:23181567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.607C>A
AA Mutation	p.Leu203Met(p.L203M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000305877
Start	23290351:23290351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201711782
CDS Mutation	c.2720C>T
AA Mutation	p.Pro907Leu(p.P907L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000305877
Start	23311830:23311830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3316G>A
AA Mutation	p.Asp1106Asn(p.D1106N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000305877
Start	23261487:23261487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781699932
CDS Mutation	c.1699C>T
AA Mutation	p.Arg567Cys(p.R567C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000305877
Start	23273764:23273764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2105A>C
AA Mutation	p.Lys702Thr(p.K702T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000305877
Start	23311728:23311728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780858887
CDS Mutation	c.3214C>T
AA Mutation	p.Arg1072Cys(p.R1072C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000305877
Start	23253909:23253909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1390C>T
AA Mutation	p.Pro464Ser(p.P464S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000305877
Start	23181681:23181681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.721G>A
AA Mutation	p.Gly241Ser(p.G241S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305877
Start	23271573:23271573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1902G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305877
Start	23289602:23289602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs56090728
CDS Mutation	c.2688G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305877
Start	23313981:23313981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374074883
CDS Mutation	c.3471G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305877
Start	23273696:23273696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2037C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000305877
Start	23181399:23181399(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.444delC
AA Mutation	p.Ala149ProfsTer30(p.A149Pfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000305877
Start	23181629:23181629(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.673delG
AA Mutation	p.Asp225MetfsTer27(p.D225Mfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000305877
Start	23285060:23285060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2265G>A
AA Mutation	p.Trp755Ter(p.W755*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript