Mutation

Primary Site >> Stomach Cancer

Gene >> TNRC6B

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000454349
Start	40315354:40315354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4750A>G
AA Mutation	p.Lys1584Glu(p.K1584E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000454349
Start	40315505:40315505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4901C>T
AA Mutation	p.Ser1634Leu(p.S1634L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000454349
Start	40266754:40266754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2524G>T
AA Mutation	p.Gly842Cys(p.G842C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000454349
Start	40285705:40285705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748167158
CDS Mutation	c.3643G>A
AA Mutation	p.Val1215Met(p.V1215M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000454349
Start	40265894:40265894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1664C>T
AA Mutation	p.Ala555Val(p.A555V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000454349
Start	40266417:40266417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2187T>G
AA Mutation	p.Asp729Glu(p.D729E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000454349
Start	40300982:40300982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3913G>A
AA Mutation	p.Val1305Ile(p.V1305I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000454349
Start	40265746:40265746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1516G>A
AA Mutation	p.Val506Ile(p.V506I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000454349
Start	40261994:40261994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.278C>T
AA Mutation	p.Pro93Leu(p.P93L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000454349
Start	40262002:40262002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.286C>T
AA Mutation	p.Arg96Cys(p.R96C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000454349
Start	40285735:40285735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3673C>T
AA Mutation	p.Arg1225Trp(p.R1225W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000454349
Start	40265669:40265669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768312489
CDS Mutation	c.1439C>T
AA Mutation	p.Thr480Met(p.T480M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000454349
Start	40322961:40322961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202053674
CDS Mutation	c.5222C>T
AA Mutation	p.Ala1741Val(p.A1741V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000454349
Start	40264967:40264967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.737A>G
AA Mutation	p.Gln246Arg(p.Q246R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000454349
Start	40265669:40265669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1439C>G
AA Mutation	p.Thr480Arg(p.T480R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000454349
Start	40266747:40266747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373711092
CDS Mutation	c.2517G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000454349
Start	40265409:40265409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1179A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000454349
Start	40315431:40315431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4827A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000454349
Start	40261917:40261917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.201C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000454349
Start	40264878:40264878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375524285
CDS Mutation	c.648C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000454349
Start	40321098:40321098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4983G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000454349
Start	40285763:40285763(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3706delC
AA Mutation	p.Gln1236ArgfsTer15(p.Q1236Rfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000454349
Start	40266476:40266476(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2251delG
AA Mutation	p.Glu751ArgfsTer41(p.E751Rfs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000454349
Start	40265349:40265349(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1124delA
AA Mutation	p.Asn375MetfsTer7(p.N375Mfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000454349
Start	40280015:40280015(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3285delT
AA Mutation	p.Phe1095LeufsTer8(p.F1095Lfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000454349
Start	40279994:40279994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3263-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript