Mutation

Primary Site >> Stomach Cancer

Gene >> SEC16A

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136476168:136476168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756764916
CDS Mutation	c.1448C>T
AA Mutation	p.Pro483Leu(p.P483L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136475668:136475668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200785473
CDS Mutation	c.1948G>A
AA Mutation	p.Ala650Thr(p.A650T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136451268:136451268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6300G>T
AA Mutation	p.Lys2100Asn(p.K2100N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136456091:136456091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5626T>C
AA Mutation	p.Trp1876Arg(p.W1876R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136459534:136459534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5213C>T
AA Mutation	p.Ala1738Val(p.A1738V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136477202:136477202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.414G>T
AA Mutation	p.Met138Ile(p.M138I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136462942:136462942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554095424
CDS Mutation	c.4838C>T
AA Mutation	p.Ser1613Leu(p.S1613L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136477434:136477434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779447176
CDS Mutation	c.182C>T
AA Mutation	p.Ala61Val(p.A61V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136464533:136464533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4333T>A
AA Mutation	p.Phe1445Ile(p.F1445I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136474485:136474485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3131T>C
AA Mutation	p.Val1044Ala(p.V1044A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136462929:136462929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4851G>C
AA Mutation	p.Glu1617Asp(p.E1617D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136475424:136475424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2192T>C
AA Mutation	p.Leu731Pro(p.L731P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136474680:136474680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2936A>G
AA Mutation	p.Asn979Ser(p.N979S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136477467:136477467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369124445
CDS Mutation	c.149C>T
AA Mutation	p.Pro50Leu(p.P50L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136474542:136474542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3074G>A
AA Mutation	p.Ser1025Asn(p.S1025N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136476519:136476519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1097C>T
AA Mutation	p.Ser366Leu(p.S366L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136475283:136475283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371427184
CDS Mutation	c.2333C>T
AA Mutation	p.Pro778Leu(p.P778L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000313050
Start	136463704:136463704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4483C>T
AA Mutation	p.Arg1495Trp(p.R1495W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313050
Start	136468440:136468440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3777T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313050
Start	136451340:136451340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776101479
CDS Mutation	c.6228G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313050
Start	136474379:136474379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs3812593
CDS Mutation	c.3237G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313050
Start	136474268:136474268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3348T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313050
Start	136464519:136464519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368514201
CDS Mutation	c.4347T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313050
Start	136447669:136447669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761131389
CDS Mutation	c.6459G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313050
Start	136477205:136477205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.411G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313050
Start	136462926:136462926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370099266
CDS Mutation	c.4854C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313050
Start	136467034:136467034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3852C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313050
Start	136474505:136474505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3111T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313050
Start	136446918:136446918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6729T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313050
Start	136475567:136475567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2049G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313050
Start	136476479:136476479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1137A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313050
Start	136475927:136475927(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1689delT
AA Mutation	p.Phe563LeufsTer9(p.F563Lfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313050
Start	136451371:136451371(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.6197delC
AA Mutation	p.Pro2066GlnfsTer76(p.P2066Qfs*76)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313050
Start	136474957:136474960(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2656_2659delTCTG
AA Mutation	p.Ser886GlyfsTer80(p.S886Gfs*80)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	35
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000313050
Start	136474925:136474957(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2659_2691delGGGATTCCAACCAGCTCTGTCCTTAGCTTGTCT
AA Mutation	p.Gly887_Ser897del(p.G887_S897del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript