Mutation

Primary Site >> Stomach Cancer

Gene >> FLT1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28384984:28384984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137937570
CDS Mutation	c.2017G>A
AA Mutation	p.Ala673Thr(p.A673T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28334031:28334031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2587C>A
AA Mutation	p.Leu863Met(p.L863M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28390087:28390087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1678C>G
AA Mutation	p.His560Asp(p.H560D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28427862:28427862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1166C>T
AA Mutation	p.Ser389Leu(p.S389L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28467123:28467123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.168A>C
AA Mutation	p.Glu56Asp(p.E56D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28389855:28389855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1910G>A
AA Mutation	p.Arg637Lys(p.R637K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28384972:28384972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2029T>G
AA Mutation	p.Ser677Ala(p.S677A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28339255:28339255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2401C>A
AA Mutation	p.Pro801Thr(p.P801T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28390065:28390065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374335323
CDS Mutation	c.1700C>T
AA Mutation	p.Pro567Leu(p.P567L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28308865:28308865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115595062
CDS Mutation	c.3698C>T
AA Mutation	p.Pro1233Leu(p.P1233L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28427845:28427845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369255421
CDS Mutation	c.1183G>A
AA Mutation	p.Val395Ile(p.V395I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28390062:28390062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745653714
CDS Mutation	c.1703C>T
AA Mutation	p.Thr568Met(p.T568M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28322874:28322874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2869C>A
AA Mutation	p.Leu957Ile(p.L957I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28322804:28322804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116741209
CDS Mutation	c.2939T>C
AA Mutation	p.Val980Ala(p.V980A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28384902:28384902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2099A>T
AA Mutation	p.Lys700Ile(p.K700I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000282397
Start	28427901:28427901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1127C>T
AA Mutation	p.Ala376Val(p.A376V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282397
Start	28427846:28427846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775108754
CDS Mutation	c.1182C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282397
Start	28329721:28329721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2601C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282397
Start	28306761:28306761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776434858
CDS Mutation	c.3732C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282397
Start	28321523:28321523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3114T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282397
Start	28427302:28427302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1293C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	stop_retained_variant
Transcription ID	ENST00000282397
Start	28303167:28303167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4017G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282397
Start	28433870:28433870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.762T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282397
Start	28303287:28303287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3897C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282397
Start	28438293:28438293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.441C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282397
Start	28467125:28467125(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.166delG
AA Mutation	p.Glu56LysfsTer12(p.E56Kfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000282397
Start	28438222:28438222(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.512delA
AA Mutation	p.Lys171SerfsTer7(p.K171Sfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript