Mutation

Primary Site >> Stomach Cancer

Gene >> SLIT1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97001227:97001227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4490G>A
AA Mutation	p.Cys1497Tyr(p.C1497Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97043005:97043005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141758146
CDS Mutation	c.2060G>A
AA Mutation	p.Arg687Gln(p.R687Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97002761:97002761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4097C>T
AA Mutation	p.Ala1366Val(p.A1366V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97004816:97004816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3587C>T
AA Mutation	p.Thr1196Met(p.T1196M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97046783:97046783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1724A>G
AA Mutation	p.Asn575Ser(p.N575S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97004202:97004202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3731G>T
AA Mutation	p.Gly1244Val(p.G1244V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97014039:97014039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753416251
CDS Mutation	c.3089A>G
AA Mutation	p.Gln1030Arg(p.Q1030R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97043458:97043458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759345991
CDS Mutation	c.1909C>T
AA Mutation	p.Arg637Cys(p.R637C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97043497:97043497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752908466
CDS Mutation	c.1870C>T
AA Mutation	p.Arg624Cys(p.R624C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266058
Start	97006660:97006660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3402T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266058
Start	97046689:97046689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs527636768
CDS Mutation	c.1818C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266058
Start	97063591:97063591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373349775
CDS Mutation	c.657C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266058
Start	97004084:97004084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749650797
CDS Mutation	c.3849G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266058
Start	97047773:97047773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1551C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266058
Start	97047719:97047719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1605T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266058
Start	97060723:97060723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.858C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266058
Start	97047698:97047698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1626G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266058
Start	97006654:97006654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3408C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266058
Start	97040105:97040105(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2180delG
AA Mutation	p.Gly727AlafsTer65(p.G727Afs*65)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266058
Start	97001333:97001333(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4384delG
AA Mutation	p.Asp1462ThrfsTer42(p.D1462Tfs*42)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript