Mutation

Primary Site >> Stomach Cancer

Gene >> SEMA3C

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265361
Start	80800785:80800785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.958C>A
AA Mutation	p.Leu320Ile(p.L320I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265361
Start	80789462:80789462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1198T>G
AA Mutation	p.Phe400Val(p.F400V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265361
Start	80765231:80765231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1367T>C
AA Mutation	p.Val456Ala(p.V456A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265361
Start	80758367:80758367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1607G>A
AA Mutation	p.Gly536Asp(p.G536D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265361
Start	80802734:80802734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.847T>G
AA Mutation	p.Phe283Val(p.F283V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265361
Start	80745063:80745063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2087C>A
AA Mutation	p.Ala696Glu(p.A696E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265361
Start	80810628:80810628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143834638
CDS Mutation	c.521C>T
AA Mutation	p.Thr174Met(p.T174M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265361
Start	80789409:80789409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1251G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265361
Start	80745137:80745137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370225417
CDS Mutation	c.2013G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265361
Start	80789442:80789442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1218C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265361
Start	80789337:80789337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1323T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000265361
Start	80744911:80744911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2239C>T
AA Mutation	p.Gln747Ter(p.Q747*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265361
Start	80748985:80748986(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1754dupA
AA Mutation	p.Asn585LysfsTer2(p.N585Kfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript