Mutation

Primary Site >> Stomach Cancer

Gene >> KAT6B

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287239
Start	75028585:75028585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568525923
CDS Mutation	c.3761G>A
AA Mutation	p.Arg1254His(p.R1254H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287239
Start	75029730:75029730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4906A>G
AA Mutation	p.Ile1636Val(p.I1636V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287239
Start	75030042:75030042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5218A>C
AA Mutation	p.Ile1740Leu(p.I1740L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000287239
Start	75029686:75029686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4862C>T
AA Mutation	p.Ala1621Val(p.A1621V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000287239
Start	75020705:75020705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2753A>G
AA Mutation	p.His918Arg(p.H918R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000287239
Start	74985173:74985173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2467C>T
AA Mutation	p.Pro823Ser(p.P823S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000287239
Start	75025087:75025087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3502C>T
AA Mutation	p.Pro1168Ser(p.P1168S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000287239
Start	75028584:75028584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3760C>T
AA Mutation	p.Arg1254Cys(p.R1254C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000287239
Start	75030981:75030981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6157C>T
AA Mutation	p.His2053Tyr(p.H2053Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000287239
Start	75030103:75030103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5279C>T
AA Mutation	p.Pro1760Leu(p.P1760L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000287239
Start	74843329:74843329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.472C>T
AA Mutation	p.Arg158Cys(p.R158C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000287239
Start	75028542:75028542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140989004
CDS Mutation	c.3718G>A
AA Mutation	p.Glu1240Lys(p.E1240K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000287239
Start	75029865:75029865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5041G>A
AA Mutation	p.Glu1681Lys(p.E1681K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000287239
Start	75030693:75030693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5869C>T
AA Mutation	p.Arg1957Trp(p.R1957W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000287239
Start	75029109:75029109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4285G>A
AA Mutation	p.Glu1429Lys(p.E1429K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000287239
Start	75029835:75029835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5011G>A
AA Mutation	p.Gly1671Ser(p.G1671S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000287239
Start	75029014:75029014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201038511
CDS Mutation	c.4190C>T
AA Mutation	p.Thr1397Met(p.T1397M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000287239
Start	74977384:74977384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550985531
CDS Mutation	c.2062G>A
AA Mutation	p.Val688Ile(p.V688I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287239
Start	75022078:75022078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3219G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287239
Start	75029702:75029702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146568876
CDS Mutation	c.4878C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287239
Start	74975783:74975783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1446T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287239
Start	75031034:75031034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6210C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287239
Start	75029681:75029681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4857C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287239
Start	75030464:75030464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5640A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287239
Start	74843367:74843367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750020725
CDS Mutation	c.510G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000287239
Start	74976012:74976012(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1679delA
AA Mutation	p.Lys560ArgfsTer73(p.K560Rfs*73)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000287239
Start	74976154:74976154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1817G>A
AA Mutation	p.Trp606Ter(p.W606*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000287239
Start	75025096:75025096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3511C>T
AA Mutation	p.Gln1171Ter(p.Q1171*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	stop_gained
Transcription ID	ENST00000287239
Start	75029702:75029702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4878C>A
AA Mutation	p.Tyr1626Ter(p.Y1626*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript