Mutation

Primary Site >> Stomach Cancer

Gene >> BICC1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373886
Start	58807031:58807031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2249A>C
AA Mutation	p.Glu750Ala(p.E750A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373886
Start	58513163:58513163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.20C>A
AA Mutation	p.Pro7His(p.P7H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000373886
Start	58788421:58788421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.598C>T
AA Mutation	p.Arg200Trp(p.R200W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373886
Start	58813971:58813971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2518A>G
AA Mutation	p.Lys840Glu(p.K840E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373886
Start	58798499:58798499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1467T>G
AA Mutation	p.Ser489Arg(p.S489R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373886
Start	58803132:58803132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2071G>A
AA Mutation	p.Ala691Thr(p.A691T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000373886
Start	58785049:58785049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.356A>C
AA Mutation	p.Lys119Thr(p.K119T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000373886
Start	58813867:58813867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2414A>T
AA Mutation	p.Glu805Val(p.E805V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000373886
Start	58796393:58796393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1233G>T
AA Mutation	p.Arg411Ser(p.R411S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000373886
Start	58800266:58800266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1798G>T
AA Mutation	p.Asp600Tyr(p.D600Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000373886
Start	58513292:58513292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748986819
CDS Mutation	c.149G>A
AA Mutation	p.Arg50His(p.R50H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000373886
Start	58803139:58803139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2078A>C
AA Mutation	p.Lys693Thr(p.K693T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000373886
Start	58817669:58817669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2641C>A
AA Mutation	p.Leu881Ile(p.L881I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000373886
Start	58801036:58801036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2005T>G
AA Mutation	p.Ser669Ala(p.S669A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000373886
Start	58813929:58813929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2476A>C
AA Mutation	p.Ser826Arg(p.S826R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000373886
Start	58793519:58793519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1083G>T
AA Mutation	p.Lys361Asn(p.K361N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000373886
Start	58813845:58813845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2392C>T
AA Mutation	p.Leu798Phe(p.L798F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373886
Start	58789363:58789363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749671574
CDS Mutation	c.702G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373886
Start	58828882:58828882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2916C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373886
Start	58787054:58787054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.519G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373886
Start	58798547:58798547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1515T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373886
Start	58513260:58513260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.117G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373886
Start	58828795:58828795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764421544
CDS Mutation	c.2829G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373886
Start	58807152:58807152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2370T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373886
Start	58803116:58803116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2055T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373886
Start	58786991:58786991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.456C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373886
Start	58787001:58787001(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.471delA
AA Mutation	p.Val158Ter(p.V158*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000373886
Start	58828888:58828888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2922G>A
AA Mutation	p.Trp974Ter(p.W974*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373886
Start	58799216:58799217(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1696dupA
AA Mutation	p.Ile566AsnfsTer44(p.I566Nfs*44)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript