Mutation

Primary Site >> Stomach Cancer

Gene >> KNTC1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333479
Start	122534689:122534689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.155C>T
AA Mutation	p.Ala52Val(p.A52V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000333479
Start	122575577:122575577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757801099
CDS Mutation	c.2417C>T
AA Mutation	p.Ala806Val(p.A806V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000333479
Start	122575573:122575573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2413T>C
AA Mutation	p.Tyr805His(p.Y805H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000333479
Start	122588716:122588716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3899T>C
AA Mutation	p.Phe1300Ser(p.F1300S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000333479
Start	122591437:122591437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4229G>A
AA Mutation	p.Arg1410His(p.R1410H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000333479
Start	122613212:122613212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5723A>C
AA Mutation	p.Lys1908Thr(p.K1908T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000333479
Start	122568328:122568328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1672G>A
AA Mutation	p.Glu558Lys(p.E558K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000333479
Start	122620544:122620544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370269719
CDS Mutation	c.6215C>T
AA Mutation	p.Pro2072Leu(p.P2072L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000333479
Start	122575635:122575635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2475G>T
AA Mutation	p.Met825Ile(p.M825I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000333479
Start	122615055:122615055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5942G>A
AA Mutation	p.Gly1981Glu(p.G1981E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333479
Start	122584969:122584969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3513T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333479
Start	122603176:122603176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5034A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333479
Start	122615074:122615074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5961G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333479
Start	122603179:122603179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5037C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333479
Start	122597773:122597773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4398T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333479
Start	122570894:122570894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1879T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000333479
Start	122603073:122603073(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4938delA
AA Mutation	p.Lys1646AsnfsTer2(p.K1646Nfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000333479
Start	122568311:122568311(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1661delT
AA Mutation	p.Leu554TyrfsTer3(p.L554Yfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000333479
Start	122590611:122590614(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4006_4009delAATT
AA Mutation	p.Asn1336ValfsTer4(p.N1336Vfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript