Mutation

Primary Site >> Stomach Cancer

Gene >> STIL

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360380
Start	47251265:47251265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3735T>A
AA Mutation	p.Asn1245Lys(p.N1245K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360380
Start	47251608:47251608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3392G>A
AA Mutation	p.Ser1131Asn(p.S1131N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360380
Start	47269801:47269801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2449G>A
AA Mutation	p.Asp817Asn(p.D817N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360380
Start	47302272:47302272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147160336
CDS Mutation	c.227C>T
AA Mutation	p.Ser76Leu(p.S76L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360380
Start	47251510:47251510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3490C>A
AA Mutation	p.Leu1164Ile(p.L1164I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360380
Start	47280515:47280515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1943G>T
AA Mutation	p.Cys648Phe(p.C648F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360380
Start	47251248:47251248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3752T>C
AA Mutation	p.Ile1251Thr(p.I1251T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360380
Start	47251592:47251592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3408A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360380
Start	47251730:47251730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3270T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360380
Start	47280397:47280397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2061A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360380
Start	47251697:47251697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3303C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360380
Start	47251214:47251214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754469508
CDS Mutation	c.3786A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360380
Start	47280793:47280793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1665C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360380
Start	47251841:47251841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3159A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360380
Start	47251637:47251637(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3363delA
AA Mutation	p.Lys1121AsnfsTer3(p.K1121Nfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360380
Start	47280729:47280729(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1729delT
AA Mutation	p.Ser577HisfsTer41(p.S577Hfs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360380
Start	47280909:47280909(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1549delC
AA Mutation	p.His517IlefsTer37(p.H517Ifs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript