Mutation

Primary Site >> Stomach Cancer

Gene >> MYT1L

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1903226:1903226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1886C>T
AA Mutation	p.Thr629Met(p.T629M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1922352:1922352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1417C>G
AA Mutation	p.Leu473Val(p.L473V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1889431:1889431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2330T>C
AA Mutation	p.Met777Thr(p.M777T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1979540:1979540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.70G>T
AA Mutation	p.Ala24Ser(p.A24S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1889425:1889425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2336A>C
AA Mutation	p.Lys779Thr(p.K779T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1922949:1922949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.820G>A
AA Mutation	p.Val274Ile(p.V274I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1889399:1889399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2362C>T
AA Mutation	p.Pro788Ser(p.P788S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1922351:1922351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1418T>G
AA Mutation	p.Leu473Arg(p.L473R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1923161:1923161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.608A>T
AA Mutation	p.Lys203Met(p.K203M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1923141:1923141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.628A>G
AA Mutation	p.Lys210Glu(p.K210E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1886557:1886557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2693C>T
AA Mutation	p.Thr898Ile(p.T898I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1922444:1922444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754747899
CDS Mutation	c.1325C>T
AA Mutation	p.Thr442Met(p.T442M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1922570:1922570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781013816
CDS Mutation	c.1199C>T
AA Mutation	p.Ala400Val(p.A400V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1809142:1809142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3106T>G
AA Mutation	p.Ser1036Ala(p.S1036A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1922632:1922632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1137G>A
AA Mutation	p.Met379Ile(p.M379I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000399161
Start	1886540:1886540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2710A>G
AA Mutation	p.Lys904Glu(p.K904E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1910251:1910251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1806C>A
AA Mutation	p.Asp602Glu(p.D602E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1979749:1979749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.29A>G
AA Mutation	p.His10Arg(p.H10R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1979746:1979746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761734045
CDS Mutation	c.32G>A
AA Mutation	p.Arg11His(p.R11H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399161
Start	1922569:1922569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373977335
CDS Mutation	c.1200G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399161
Start	1903159:1903159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369595125
CDS Mutation	c.1953C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399161
Start	1922656:1922656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750512584
CDS Mutation	c.1113G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399161
Start	1923049:1923049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376523179
CDS Mutation	c.720C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399161
Start	1903222:1903222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745509992
CDS Mutation	c.1890G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399161
Start	1979742:1979742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs544383762
CDS Mutation	c.36G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399161
Start	1839223:1839223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375638505
CDS Mutation	c.3006G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399161
Start	1886550:1886550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2700C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399161
Start	1922314:1922314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1455C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399161
Start	1889319:1889319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372483670
CDS Mutation	c.2442C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399161
Start	1851661:1851661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2754C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399161
Start	1922595:1922595(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1174delC
AA Mutation	p.Arg392GlyfsTer24(p.R392Gfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399161
Start	1917296:1917296(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1527delC
AA Mutation	p.Cys511ValfsTer7(p.C511Vfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399161
Start	1922302:1922303(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1466dupA
AA Mutation	p.Pro490AlafsTer5(p.P490Afs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	34
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000399161
Start	1792352:1792363(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3378_3389delGTCTCTGATCCA
AA Mutation	p.Gln1126_Ile1129del(p.Q1126_I1129del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript