Mutation

Primary Site >> Stomach Cancer

Gene >> MYT1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64217092:64217092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777697773
CDS Mutation	c.1657G>A
AA Mutation	p.Glu553Lys(p.E553K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64239796:64239796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777946857
CDS Mutation	c.3130G>A
AA Mutation	p.Glu1044Lys(p.E1044K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64218940:64218940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1876G>T
AA Mutation	p.Ala626Ser(p.A626S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64239875:64239875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3209G>C
AA Mutation	p.Ser1070Thr(p.S1070T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64207888:64207888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139069988
CDS Mutation	c.692G>A
AA Mutation	p.Arg231His(p.R231H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64221981:64221981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2330G>A
AA Mutation	p.Gly777Glu(p.G777E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64208416:64208416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1220A>G
AA Mutation	p.Gln407Arg(p.Q407R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64227428:64227428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755397766
CDS Mutation	c.2542G>A
AA Mutation	p.Gly848Ser(p.G848S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64205564:64205564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.161G>A
AA Mutation	p.Cys54Tyr(p.C54Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64221972:64221972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2321A>C
AA Mutation	p.Lys774Thr(p.K774T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64221977:64221977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2326C>G
AA Mutation	p.Pro776Ala(p.P776A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64232247:64232247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770439955
CDS Mutation	c.2759C>T
AA Mutation	p.Ala920Val(p.A920V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64205069:64205069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766732552
CDS Mutation	c.121G>A
AA Mutation	p.Val41Ile(p.V41I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64217117:64217117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759933398
CDS Mutation	c.1682G>A
AA Mutation	p.Arg561Gln(p.R561Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64205775:64205775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.372G>C
AA Mutation	p.Glu124Asp(p.E124D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000328439
Start	64218940:64218940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1876G>A
AA Mutation	p.Ala626Thr(p.A626T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328439
Start	64217079:64217079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1644C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328439
Start	64217196:64217196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779615817
CDS Mutation	c.1761C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328439
Start	64208297:64208297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148738850
CDS Mutation	c.1101G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328439
Start	64239882:64239882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3216C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328439
Start	64208408:64208408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1212G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328439
Start	64239765:64239765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3099C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328439
Start	64207634:64207634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142929665
CDS Mutation	c.438C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328439
Start	64205721:64205721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.318T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328439
Start	64217154:64217154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1719G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328439
Start	64208105:64208105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.909G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000328439
Start	64205722:64205722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.319G>T
AA Mutation	p.Glu107Ter(p.E107*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000328439
Start	64219720:64219721(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1988_1989insTAGGGTTAGGGTTATCGAGGT
AA Mutation	p.Val663_Asp664insArgValArgValIleGluVal(p.V663_D664insRVRVIEV)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript