Mutation

Primary Site >> Stomach Cancer

Gene >> NRG3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000404547
Start	82951555:82951555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1141T>C
AA Mutation	p.Phe381Leu(p.F381L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000404547
Start	82985267:82985267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757686427
CDS Mutation	c.1825A>C
AA Mutation	p.Thr609Pro(p.T609P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000404547
Start	82358742:82358742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760046822
CDS Mutation	c.827C>T
AA Mutation	p.Thr276Met(p.T276M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000404547
Start	82985589:82985589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2147C>A
AA Mutation	p.Ser716Tyr(p.S716Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000404547
Start	81876091:81876091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.751G>A
AA Mutation	p.Ala251Thr(p.A251T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000404547
Start	82951544:82951544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1130T>A
AA Mutation	p.Phe377Tyr(p.F377Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000404547
Start	81875711:81875711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.371C>T
AA Mutation	p.Ala124Val(p.A124V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000404547
Start	82959011:82959011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1220T>C
AA Mutation	p.Leu407Pro(p.L407P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000404547
Start	82951505:82951505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1091T>G
AA Mutation	p.Ile364Ser(p.I364S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000404547
Start	82985201:82985201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1759C>A
AA Mutation	p.Leu587Met(p.L587M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000404547
Start	82358822:82358822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764611896
CDS Mutation	c.907G>A
AA Mutation	p.Glu303Lys(p.E303K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000404547
Start	82738615:82738615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.992T>G
AA Mutation	p.Phe331Cys(p.F331C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000404547
Start	81875828:81875828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.488G>T
AA Mutation	p.Arg163Leu(p.R163L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000404547
Start	81875870:81875870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.530C>T
AA Mutation	p.Ala177Val(p.A177V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000404547
Start	81875752:81875752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.412G>A
AA Mutation	p.Ala138Thr(p.A138T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000404547
Start	81875764:81875764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.424G>A
AA Mutation	p.Ala142Thr(p.A142T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000404547
Start	82979077:82979077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564020344
CDS Mutation	c.1540G>A
AA Mutation	p.Glu514Lys(p.E514K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000404547
Start	82985322:82985322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1880A>C
AA Mutation	p.Asn627Thr(p.N627T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000404547
Start	82951479:82951479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1065A>C
AA Mutation	p.Glu355Asp(p.E355D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000404547
Start	82985228:82985228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1786A>G
AA Mutation	p.Ser596Gly(p.S596G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000404547
Start	81875893:81875893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.553C>T
AA Mutation	p.Arg185Trp(p.R185W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000404547
Start	82985288:82985288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1846A>G
AA Mutation	p.Ile616Val(p.I616V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404547
Start	82985554:82985554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759140331
CDS Mutation	c.2112G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404547
Start	81875619:81875619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.279C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404547
Start	82985203:82985203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1761G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404547
Start	82985446:82985446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2004C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404547
Start	82738589:82738589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.966C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404547
Start	82738622:82738622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.999G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404547
Start	81875583:81875583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.243C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404547
Start	81875739:81875739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.399C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404547
Start	81875904:81875904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.564G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404547
Start	82985200:82985200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1758C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000404547
Start	82959015:82959054(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1227_1266delATCCAGCACAATGGCAAAGTCAGAGAACTTGGTGAAGAGC
AA Mutation	p.Ser410MetfsTer15(p.S410Mfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000404547
Start	81875482:81875482(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.148delC
AA Mutation	p.Arg50GlyfsTer53(p.R50Gfs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript