Mutation

Primary Site >> Stomach Cancer

Gene >> NRIP1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000318948
Start	14967652:14967652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748383151
CDS Mutation	c.541G>A
AA Mutation	p.Ala181Thr(p.A181T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000318948
Start	14967973:14967973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.220C>A
AA Mutation	p.Gln74Lys(p.Q74K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000318948
Start	14967514:14967514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.679A>G
AA Mutation	p.Thr227Ala(p.T227A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000318948
Start	14965245:14965245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2948G>A
AA Mutation	p.Gly983Glu(p.G983E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000318948
Start	14964944:14964944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3249A>C
AA Mutation	p.Glu1083Asp(p.E1083D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000318948
Start	14964948:14964948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3245G>A
AA Mutation	p.Arg1082Gln(p.R1082Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000318948
Start	14967291:14967291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.902T>C
AA Mutation	p.Met301Thr(p.M301T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000318948
Start	14965470:14965470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2723A>G
AA Mutation	p.Glu908Gly(p.E908G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000318948
Start	14965731:14965731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774507180
CDS Mutation	c.2462G>A
AA Mutation	p.Arg821Gln(p.R821Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000318948
Start	14967865:14967865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755926461
CDS Mutation	c.328G>A
AA Mutation	p.Val110Ile(p.V110I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000318948
Start	14967643:14967643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.550C>T
AA Mutation	p.His184Tyr(p.H184Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000318948
Start	14967136:14967136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1057A>T
AA Mutation	p.Ile353Phe(p.I353F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000318948
Start	14967675:14967675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.518A>C
AA Mutation	p.Lys173Thr(p.K173T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000318948
Start	14966468:14966468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1725C>G
AA Mutation	p.Ile575Met(p.I575M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000318948
Start	14967333:14967333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150993445
CDS Mutation	c.860C>T
AA Mutation	p.Thr287Met(p.T287M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318948
Start	14967332:14967332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768366141
CDS Mutation	c.861G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318948
Start	14967704:14967704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.489C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318948
Start	14965820:14965820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747131187
CDS Mutation	c.2373C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000318948
Start	14966396:14966396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1797A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000318948
Start	14966009:14966009(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs776154715
CDS Mutation	c.2184delA
AA Mutation	p.Glu729ArgfsTer5(p.E729Rfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000318948
Start	14966646:14966646(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1547delA
AA Mutation	p.Asn516ThrfsTer11(p.N516Tfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000318948
Start	14967117:14967117(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1076delA
AA Mutation	p.Asn359MetfsTer13(p.N359Mfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript