Mutation

Primary Site >> Stomach Cancer

Gene >> NELFCD

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000602795
Start	58989937:58989937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373372450
CDS Mutation	c.791G>A
AA Mutation	p.Gly264Asp(p.G264D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000602795
Start	58990986:58990986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.919G>A
AA Mutation	p.Ala307Thr(p.A307T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000602795
Start	58989883:58989883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.737C>T
AA Mutation	p.Thr246Met(p.T246M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000602795
Start	58993706:58993706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1577G>A
AA Mutation	p.Arg526Gln(p.R526Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000602795
Start	58991370:58991370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1067G>A
AA Mutation	p.Arg356Gln(p.R356Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000602795
Start	58993733:58993733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1604A>G
AA Mutation	p.Asp535Gly(p.D535G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000602795
Start	58986805:58986805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.282A>C
AA Mutation	p.Glu94Asp(p.E94D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000602795
Start	58994657:58994657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1781A>C
AA Mutation	p.Asn594Thr(p.N594T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000602795
Start	58986815:58986815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751386529
CDS Mutation	c.292G>A
AA Mutation	p.Ala98Thr(p.A98T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000602795
Start	58989954:58989954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.808A>T
AA Mutation	p.Ile270Phe(p.I270F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000602795
Start	58993002:58993002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1288C>G
AA Mutation	p.Pro430Ala(p.P430A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000602795
Start	58993099:58993099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371084351
CDS Mutation	c.1385C>T
AA Mutation	p.Ala462Val(p.A462V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000602795
Start	58991425:58991425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143108259
CDS Mutation	c.1122C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000602795
Start	58993695:58993695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1566C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000602795
Start	58989932:58989932(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.791delG
AA Mutation	p.Gly264AlafsTer27(p.G264Afs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000602795
Start	58993705:58993705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1576C>T
AA Mutation	p.Arg526Ter(p.R526*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript