Mutation

Primary Site >> Stomach Cancer

Gene >> RBBP6

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319715
Start	24568822:24568822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758145892
CDS Mutation	c.2132G>A
AA Mutation	p.Arg711His(p.R711H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319715
Start	24571421:24571421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138495629
CDS Mutation	c.4355C>T
AA Mutation	p.Thr1452Met(p.T1452M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000319715
Start	24567798:24567798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1959G>T
AA Mutation	p.Lys653Asn(p.K653N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000319715
Start	24569230:24569230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767988268
CDS Mutation	c.2540C>T
AA Mutation	p.Ala847Val(p.A847V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000319715
Start	24570344:24570344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3654A>C
AA Mutation	p.Lys1218Asn(p.K1218N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000319715
Start	24568828:24568828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2138G>A
AA Mutation	p.Arg713His(p.R713H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000319715
Start	24571778:24571778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4712A>C
AA Mutation	p.Lys1571Thr(p.K1571T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000319715
Start	24571669:24571669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4603A>G
AA Mutation	p.Ser1535Gly(p.S1535G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000319715
Start	24570460:24570460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3770G>A
AA Mutation	p.Gly1257Glu(p.G1257E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000319715
Start	24540709:24540709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.83A>C
AA Mutation	p.Asp28Ala(p.D28A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000319715
Start	24567336:24567336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199538396
CDS Mutation	c.1783G>A
AA Mutation	p.Ala595Thr(p.A595T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000319715
Start	24570980:24570980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148664608
CDS Mutation	c.3914C>T
AA Mutation	p.Ala1305Val(p.A1305V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000319715
Start	24571561:24571561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4495G>A
AA Mutation	p.Asp1499Asn(p.D1499N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000319715
Start	24569431:24569431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2741C>G
AA Mutation	p.Thr914Arg(p.T914R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000319715
Start	24555862:24555862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770951060
CDS Mutation	c.479C>T
AA Mutation	p.Thr160Met(p.T160M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000319715
Start	24568954:24568954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199798897
CDS Mutation	c.2264G>A
AA Mutation	p.Arg755Gln(p.R755Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000319715
Start	24568774:24568774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2084A>G
AA Mutation	p.Tyr695Cys(p.Y695C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000319715
Start	24569430:24569430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2740A>G
AA Mutation	p.Thr914Ala(p.T914A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000319715
Start	24569970:24569970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3280A>G
AA Mutation	p.Lys1094Glu(p.K1094E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000319715
Start	24567874:24567874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757145338
CDS Mutation	c.2035C>T
AA Mutation	p.Arg679Cys(p.R679C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000319715
Start	24556447:24556447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.674C>T
AA Mutation	p.Ala225Val(p.A225V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000319715
Start	24572204:24572204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374147465
CDS Mutation	c.5138G>A
AA Mutation	p.Ser1713Asn(p.S1713N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319715
Start	24567356:24567356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1803T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319715
Start	24567224:24567224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1671A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319715
Start	24569774:24569774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3084G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319715
Start	24570269:24570269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3579G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000319715
Start	24571483:24571483(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4423delA
AA Mutation	p.Thr1475LeufsTer20(p.T1475Lfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000319715
Start	24571300:24571300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4234G>T
AA Mutation	p.Glu1412Ter(p.E1412*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000319715
Start	24571875:24571876(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4810dupA
AA Mutation	p.Thr1604AsnfsTer5(p.T1604Nfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	30
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000319715
Start	24567506:24567506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1952+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript