Mutation

Primary Site >> Stomach Cancer

Gene >> YTHDF1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370339
Start	63203800:63203800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779046558
CDS Mutation	c.140G>A
AA Mutation	p.Ser47Asn(p.S47N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370339
Start	63202294:63202294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1646T>C
AA Mutation	p.Val549Ala(p.V549A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370339
Start	63202729:63202729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1211G>A
AA Mutation	p.Arg404His(p.R404H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370339
Start	63203183:63203183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543127893
CDS Mutation	c.757G>A
AA Mutation	p.Gly253Arg(p.G253R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370339
Start	63202300:63202300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749778238
CDS Mutation	c.1640A>T
AA Mutation	p.Glu547Val(p.E547V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370339
Start	63203558:63203558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.382G>A
AA Mutation	p.Ala128Thr(p.A128T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000370339
Start	63203317:63203317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.623G>A
AA Mutation	p.Ser208Asn(p.S208N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000370339
Start	63203578:63203578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.362A>T
AA Mutation	p.Asn121Ile(p.N121I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000370339
Start	63203735:63203735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.205T>C
AA Mutation	p.Ser69Pro(p.S69P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000370339
Start	63196726:63196726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1662G>C
AA Mutation	p.Gln554His(p.Q554H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000370339
Start	63202315:63202315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759033271
CDS Mutation	c.1625G>A
AA Mutation	p.Arg542His(p.R542H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000370339
Start	63202640:63202640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149076716
CDS Mutation	c.1300G>A
AA Mutation	p.Val434Ile(p.V434I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370339
Start	63202491:63202491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763697350
CDS Mutation	c.1449T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370339
Start	63202935:63202935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753193369
CDS Mutation	c.1005C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370339
Start	63202881:63202881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765559966
CDS Mutation	c.1059C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370339
Start	63213909:63213909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.87T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370339
Start	63203673:63203673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752258620
CDS Mutation	c.267C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370339
Start	63203616:63203616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.324T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370339
Start	63203572:63203572(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.368delT
AA Mutation	p.Phe123SerfsTer58(p.F123Sfs*58)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000370339
Start	63202697:63202697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1243G>T
AA Mutation	p.Glu415Ter(p.E415*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript