Mutation

Primary Site >> Stomach Cancer

Gene >> FMNL2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000288670
Start	152628529:152628529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2396C>T
AA Mutation	p.Thr799Ile(p.T799I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000288670
Start	152619154:152619154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1623A>C
AA Mutation	p.Glu541Asp(p.E541D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000288670
Start	152629713:152629713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2458A>G
AA Mutation	p.Lys820Glu(p.K820E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000288670
Start	152521982:152521982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375469230
CDS Mutation	c.157C>T
AA Mutation	p.Arg53Trp(p.R53W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000288670
Start	152618874:152618874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1343T>C
AA Mutation	p.Val448Ala(p.V448A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000288670
Start	152542805:152542805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.268G>A
AA Mutation	p.Ala90Thr(p.A90T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000288670
Start	152614971:152614971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1183G>A
AA Mutation	p.Val395Met(p.V395M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000288670
Start	152619698:152619698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1817T>C
AA Mutation	p.Val606Ala(p.V606A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000288670
Start	152628345:152628345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543308996
CDS Mutation	c.2212C>T
AA Mutation	p.Arg738Trp(p.R738W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000288670
Start	152614902:152614902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1114C>A
AA Mutation	p.Leu372Met(p.L372M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000288670
Start	152335665:152335665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.62T>C
AA Mutation	p.Leu21Ser(p.L21S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288670
Start	152626701:152626701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2139T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288670
Start	152619016:152619016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1485A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000288670
Start	152632074:152632074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2617G>T
AA Mutation	p.Glu873Ter(p.E873*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript