Mutation

Primary Site >> Stomach Cancer

Gene >> DOT1L

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398665
Start	2210738:2210738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1234G>A
AA Mutation	p.Gly412Arg(p.G412R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000398665
Start	2216575:2216575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2218G>A
AA Mutation	p.Ala740Thr(p.A740T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000398665
Start	2210670:2210670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1166C>A
AA Mutation	p.Pro389Gln(p.P389Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000398665
Start	2222222:2222222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3053G>A
AA Mutation	p.Gly1018Asp(p.G1018D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000398665
Start	2202761:2202761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.769T>C
AA Mutation	p.Phe257Leu(p.F257L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000398665
Start	2216632:2216632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769937964
CDS Mutation	c.2275C>T
AA Mutation	p.Arg759Cys(p.R759C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000398665
Start	2191078:2191078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.331C>A
AA Mutation	p.Leu111Met(p.L111M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000398665
Start	2211119:2211119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1372A>G
AA Mutation	p.Ser458Gly(p.S458G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000398665
Start	2222336:2222336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3167C>T
AA Mutation	p.Ala1056Val(p.A1056V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000398665
Start	2217875:2217875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2648T>C
AA Mutation	p.Ile883Thr(p.I883T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000398665
Start	2191100:2191100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.353C>T
AA Mutation	p.Ser118Leu(p.S118L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000398665
Start	2191018:2191018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271G>T
AA Mutation	p.Gly91Cys(p.G91C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000398665
Start	2211141:2211141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778851336
CDS Mutation	c.1394C>T
AA Mutation	p.Pro465Leu(p.P465L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398665
Start	2226928:2226928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4407G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398665
Start	2222100:2222100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762151259
CDS Mutation	c.2931C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398665
Start	2226316:2226316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371535945
CDS Mutation	c.3795C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398665
Start	2213583:2213583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1602C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398665
Start	2217888:2217888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768292906
CDS Mutation	c.2661C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398665
Start	2199895:2199895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.663C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398665
Start	2194556:2194556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.630A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398665
Start	2226523:2226523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4002T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000398665
Start	2226424:2226424(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3907delG
AA Mutation	p.Ala1303LeufsTer24(p.A1303Lfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000398665
Start	2191142:2191142(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.399delC
AA Mutation	p.Glu134ArgfsTer14(p.E134Rfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000398665
Start	2210767:2210767(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1266delC
AA Mutation	p.Glu423SerfsTer66(p.E423Sfs*66)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000398665
Start	2226587:2226587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4066C>T
AA Mutation	p.Gln1356Ter(p.Q1356*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000398665
Start	2193688:2193688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.494-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	27
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000398665
Start	2213892:2213894(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1705_1707delAAG
AA Mutation	p.Lys569del(p.K569del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript