Mutation

Primary Site >> Stomach Cancer

Gene >> FLOT2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394908
Start	28888955:28888955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775401852
CDS Mutation	c.121G>A
AA Mutation	p.Asp41Asn(p.D41N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394908
Start	28884238:28884238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749079749
CDS Mutation	c.209C>T
AA Mutation	p.Thr70Met(p.T70M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000394908
Start	28883130:28883130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.324G>T
AA Mutation	p.Glu108Asp(p.E108D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000394908
Start	28897541:28897541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.34G>A
AA Mutation	p.Ala12Thr(p.A12T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000394908
Start	28882623:28882623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.415G>A
AA Mutation	p.Ala139Thr(p.A139T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000394908
Start	28881989:28881989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567172028
CDS Mutation	c.739C>T
AA Mutation	p.Arg247Cys(p.R247C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000394908
Start	28881869:28881869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756020730
CDS Mutation	c.859C>T
AA Mutation	p.Arg287Cys(p.R287C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394908
Start	28881825:28881825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.903C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394908
Start	28882349:28882349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537594430
CDS Mutation	c.567C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394908
Start	28880757:28880757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1204C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394908
Start	28884254:28884254(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.193delG
AA Mutation	p.Val65Ter(p.V65*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	12
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000394908
Start	28881812:28881812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.914+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript