Mutation

Primary Site >> Stomach Cancer

Gene >> NEDD9

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379446
Start	11213298:11213298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.442C>T
AA Mutation	p.Pro148Ser(p.P148S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379446
Start	11190923:11190923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.946G>A
AA Mutation	p.Ala316Thr(p.A316T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379446
Start	11185494:11185494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2173G>A
AA Mutation	p.Ala725Thr(p.A725T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379446
Start	11185485:11185485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760782051
CDS Mutation	c.2182G>A
AA Mutation	p.Ala728Thr(p.A728T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379446
Start	11185598:11185598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2069C>G
AA Mutation	p.Ser690Cys(p.S690C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000379446
Start	11191133:11191133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.736C>T
AA Mutation	p.Pro246Ser(p.P246S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000379446
Start	11190134:11190134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1735T>C
AA Mutation	p.Tyr579His(p.Y579H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000379446
Start	11193626:11193626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773292318
CDS Mutation	c.526G>A
AA Mutation	p.Val176Ile(p.V176I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379446
Start	11191167:11191167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.702A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379446
Start	11190813:11190813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs575153183
CDS Mutation	c.1056G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379446
Start	11190570:11190570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199667749
CDS Mutation	c.1299C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379446
Start	11193681:11193681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560578781
CDS Mutation	c.471C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379446
Start	11192357:11192357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs76565582
CDS Mutation	c.651G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379446
Start	11190213:11190213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576943272
CDS Mutation	c.1656C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379446
Start	11190252:11190252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146690144
CDS Mutation	c.1617C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379446
Start	11190966:11190966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.903C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000379446
Start	11190620:11190620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1249C>T
AA Mutation	p.Gln417Ter(p.Q417*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000379446
Start	11185363:11185383(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2284_2304delACGCTGACACGGCAGGTGACT
AA Mutation	p.Thr762_Thr768del(p.T762_T768del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript