Mutation

Primary Site >> Stomach Cancer

Gene >> NELL2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000429094
Start	44532637:44532637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1748G>T
AA Mutation	p.Cys583Phe(p.C583F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000429094
Start	44523320:44523320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1969A>T
AA Mutation	p.Asn657Tyr(p.N657Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000429094
Start	44774773:44774773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757940415
CDS Mutation	c.968A>G
AA Mutation	p.Asp323Gly(p.D323G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000429094
Start	44665588:44665588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1340G>A
AA Mutation	p.Gly447Glu(p.G447E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000429094
Start	44779999:44779999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753991527
CDS Mutation	c.359G>A
AA Mutation	p.Gly120Asp(p.G120D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000429094
Start	44777244:44777244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771170673
CDS Mutation	c.677G>A
AA Mutation	p.Arg226His(p.R226H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000429094
Start	44779922:44779922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.436G>T
AA Mutation	p.Ala146Ser(p.A146S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000429094
Start	44779849:44779849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.509A>G
AA Mutation	p.Lys170Arg(p.K170R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000429094
Start	44714699:44714699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1037G>C
AA Mutation	p.Arg346Thr(p.R346T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000429094
Start	44522077:44522077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2098T>C
AA Mutation	p.Cys700Arg(p.C700R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000429094
Start	44816104:44816104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.217A>G
AA Mutation	p.Thr73Ala(p.T73A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000429094
Start	44779954:44779954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202194885
CDS Mutation	c.404G>A
AA Mutation	p.Arg135His(p.R135H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000429094
Start	44522109:44522109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2066G>A
AA Mutation	p.Cys689Tyr(p.C689Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000429094
Start	44777091:44777091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.713T>C
AA Mutation	p.Val238Ala(p.V238A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000429094
Start	44610892:44610892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1523G>A
AA Mutation	p.Cys508Tyr(p.C508Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000429094
Start	44875289:44875289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.120G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000429094
Start	44522075:44522075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2100C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000429094
Start	44523438:44523438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1851C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000429094
Start	44523345:44523345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762324368
CDS Mutation	c.1944C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000429094
Start	44522126:44522126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2049A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000429094
Start	44714653:44714653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1083C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000429094
Start	44520013:44520013(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2392delC
AA Mutation	p.Gln798SerfsTer30(p.Q798Sfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000429094
Start	44532708:44532708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1677C>A
AA Mutation	p.Cys559Ter(p.C559*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript