Mutation

Primary Site >> Stomach Cancer

Gene >> RUNX1T1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265814
Start	91986223:91986223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200248598
CDS Mutation	c.1180C>T
AA Mutation	p.Arg394Trp(p.R394W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265814
Start	92011037:92011037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.523T>G
AA Mutation	p.Phe175Val(p.F175V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265814
Start	91970785:91970785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1412C>T
AA Mutation	p.Ala471Val(p.A471V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265814
Start	91986222:91986222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759634592
CDS Mutation	c.1181G>A
AA Mutation	p.Arg394Gln(p.R394Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265814
Start	92017283:92017283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759112769
CDS Mutation	c.169C>T
AA Mutation	p.Pro57Ser(p.P57S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265814
Start	91986220:91986220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1183C>T
AA Mutation	p.Arg395Trp(p.R395W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265814
Start	91991875:91991875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.755G>A
AA Mutation	p.Gly252Asp(p.G252D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265814
Start	91986183:91986183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1220G>A
AA Mutation	p.Gly407Asp(p.G407D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265814
Start	91986963:91986963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1001G>A
AA Mutation	p.Gly334Asp(p.G334D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265814
Start	91986274:91986274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1129G>A
AA Mutation	p.Val377Ile(p.V377I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000265814
Start	92017240:92017240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.212T>C
AA Mutation	p.Phe71Ser(p.F71S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000265814
Start	91975943:91975943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377029087
CDS Mutation	c.1310C>T
AA Mutation	p.Ala437Val(p.A437V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000265814
Start	91986265:91986265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1138C>T
AA Mutation	p.Arg380Trp(p.R380W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000265814
Start	92005297:92005297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777373997
CDS Mutation	c.559G>A
AA Mutation	p.Ala187Thr(p.A187T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265814
Start	92014735:92014735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775861396
CDS Mutation	c.312T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265814
Start	91970784:91970784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142225049
CDS Mutation	c.1413G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265814
Start	91986146:91986146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1257C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265814
Start	92017311:92017311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760199416
CDS Mutation	c.141G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265814
Start	91991793:91991793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.837T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265814
Start	92075999:92075999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.54C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265814
Start	92017347:92017347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.105C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265814
Start	91960404:91960404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1653T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265814
Start	92075987:92075987(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.66delA
AA Mutation	p.Asn24ThrfsTer22(p.N24Tfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265814
Start	92014774:92014774(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.273delC
AA Mutation	p.Ser92HisfsTer35(p.S92Hfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000265814
Start	91986286:91986286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1117C>T
AA Mutation	p.Arg373Ter(p.R373*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000265814
Start	91991890:91991890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.741-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	27
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000265814
Start	91991638:91991638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.991+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript