Mutation

Primary Site >> Stomach Cancer

Gene >> NEDD4L

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000400345
Start	58335518:58335518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199527463
CDS Mutation	c.1106C>T
AA Mutation	p.Thr369Met(p.T369M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000400345
Start	58390680:58390680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2690G>A
AA Mutation	p.Arg897Gln(p.R897Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000400345
Start	58391526:58391526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2792G>C
AA Mutation	p.Gly931Ala(p.G931A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000400345
Start	58329018:58329018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.704A>T
AA Mutation	p.Asn235Ile(p.N235I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000400345
Start	58385563:58385563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2464A>G
AA Mutation	p.Lys822Glu(p.K822E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400345
Start	58341791:58341791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369600630
CDS Mutation	c.1371G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400345
Start	58329106:58329106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750888753
CDS Mutation	c.792G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400345
Start	58252051:58252051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.294A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400345
Start	58333853:58333853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1026T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000400345
Start	58323283:58323283(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.467delA
AA Mutation	p.Asn156MetfsTer51(p.N156Mfs*51)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000400345
Start	58341137:58341137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1225C>T
AA Mutation	p.Arg409Ter(p.R409*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript