Mutation

Primary Site >> Stomach Cancer

Gene >> SEMA3E

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83367665:83367665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2249A>G
AA Mutation	p.Lys750Arg(p.K750R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83400129:83400129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1265C>A
AA Mutation	p.Pro422Gln(p.P422Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83408472:83408472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765052488
CDS Mutation	c.566C>T
AA Mutation	p.Ala189Val(p.A189V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83368016:83368016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1898T>C
AA Mutation	p.Val633Ala(p.V633A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83406006:83406006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.867A>T
AA Mutation	p.Lys289Asn(p.K289N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83490175:83490175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.215T>C
AA Mutation	p.Val72Ala(p.V72A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83469284:83469284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.295G>A
AA Mutation	p.Ala99Thr(p.A99T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83407180:83407180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.730G>A
AA Mutation	p.Val244Ile(p.V244I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000307792
Start	83469244:83469244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780025635
CDS Mutation	c.335C>T
AA Mutation	p.Ala112Val(p.A112V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83648532:83648532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751165516
CDS Mutation	c.11C>T
AA Mutation	p.Ala4Val(p.A4V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83418441:83418441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.499A>G
AA Mutation	p.Arg167Gly(p.R167G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83367822:83367822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2092G>T
AA Mutation	p.Ala698Ser(p.A698S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83367599:83367599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766002060
CDS Mutation	c.2315C>T
AA Mutation	p.Thr772Met(p.T772M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83367768:83367768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2146C>A
AA Mutation	p.Leu716Met(p.L716M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83392585:83392585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1637G>A
AA Mutation	p.Arg546Gln(p.R546Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83408380:83408380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371604308
CDS Mutation	c.658C>T
AA Mutation	p.Arg220Cys(p.R220C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000307792
Start	83466556:83466556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.382A>T
AA Mutation	p.Thr128Ser(p.T128S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307792
Start	83402713:83402713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201719889
CDS Mutation	c.1062C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307792
Start	83408387:83408387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766680673
CDS Mutation	c.651C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307792
Start	83400221:83400221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370540865
CDS Mutation	c.1173C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307792
Start	83490234:83490234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.156T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307792
Start	83400115:83400115(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1279delA
AA Mutation	p.Thr427GlnfsTer7(p.T427Qfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307792
Start	83405507:83405507(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.941delT
AA Mutation	p.Leu314CysfsTer11(p.L314Cfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript