Mutation

Primary Site >> Stomach Cancer

Gene >> NUP88

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000573584
Start	5404144:5404144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1147G>C
AA Mutation	p.Asp383His(p.D383H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000573584
Start	5387440:5387440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774967326
CDS Mutation	c.1862G>A
AA Mutation	p.Arg621His(p.R621H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000573584
Start	5387864:5387864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1684C>T
AA Mutation	p.Leu562Phe(p.L562F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000573584
Start	5410744:5410744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.639A>G
AA Mutation	p.Ile213Met(p.I213M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000573584
Start	5386804:5386804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2066A>G
AA Mutation	p.Gln689Arg(p.Q689R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000573584
Start	5405189:5405189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.912A>C
AA Mutation	p.Glu304Asp(p.E304D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000573584
Start	5419392:5419392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.259A>G
AA Mutation	p.Ser87Gly(p.S87G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000573584
Start	5388886:5388886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149123666
CDS Mutation	c.1559G>A
AA Mutation	p.Arg520His(p.R520H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000573584
Start	5408904:5408904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770092360
CDS Mutation	c.686C>T
AA Mutation	p.Ala229Val(p.A229V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000573584
Start	5408897:5408897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.693C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000573584
Start	5408786:5408786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.804C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000573584
Start	5419387:5419387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.264C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000573584
Start	5419612:5419612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.39G>A
Mutation Classification	Silent
Feature Type	Transcript