Mutation

Primary Site >> Stomach Cancer

Gene >> NETO2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000562435
Start	47083612:47083612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1187C>T
AA Mutation	p.Pro396Leu(p.P396L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000562435
Start	47083523:47083523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772817589
CDS Mutation	c.1276C>T
AA Mutation	p.Arg426Trp(p.R426W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000562435
Start	47109527:47109527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.839G>A
AA Mutation	p.Ser280Asn(p.S280N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000562435
Start	47128532:47128532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746342583
CDS Mutation	c.274T>C
AA Mutation	p.Tyr92His(p.Y92H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000562435
Start	47109605:47109605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.761A>C
AA Mutation	p.Lys254Thr(p.K254T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000562435
Start	47083585:47083585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1214A>G
AA Mutation	p.Asp405Gly(p.D405G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000562435
Start	47128340:47128340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.466T>C
AA Mutation	p.Tyr156His(p.Y156H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000562435
Start	47128413:47128413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781699946
CDS Mutation	c.393A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000562435
Start	47083638:47083638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771545207
CDS Mutation	c.1161C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000562435
Start	47122774:47122774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748318682
CDS Mutation	c.537C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000562435
Start	47109652:47109652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139454743
CDS Mutation	c.714C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000562435
Start	47083335:47083335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1464A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000562435
Start	47122663:47122663(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.648delA
AA Mutation	p.Ala217LeufsTer5(p.A217Lfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000562435
Start	47086237:47086237(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.986delA
AA Mutation	p.Asn329IlefsTer39(p.N329Ifs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000562435
Start	47129308:47129308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.148C>T
AA Mutation	p.Arg50Ter(p.R50*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000562435
Start	47086236:47086237(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.986dupA
AA Mutation	p.Asn329LysfsTer4(p.N329Kfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript