Mutation

Primary Site >> Liver Cancer

Gene >> MYT1L

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1917217:1917217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1606G>A
AA Mutation	p.Val536Ile(p.V536I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1922300:1922300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1469C>A
AA Mutation	p.Pro490Gln(p.P490Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1839293:1839293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2936C>G
AA Mutation	p.Pro979Arg(p.P979R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1892143:1892143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2177T>G
AA Mutation	p.Met726Arg(p.M726R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1922402:1922402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756469250
CDS Mutation	c.1367C>T
AA Mutation	p.Ala456Val(p.A456V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1922966:1922966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.803T>C
AA Mutation	p.Leu268Ser(p.L268S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1922657:1922657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573013583
CDS Mutation	c.1112C>T
AA Mutation	p.Thr371Met(p.T371M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1922597:1922597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1172C>A
AA Mutation	p.Pro391His(p.P391H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1892098:1892098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2222C>T
AA Mutation	p.Thr741Met(p.T741M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1809115:1809115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774591482
CDS Mutation	c.3133G>A
AA Mutation	p.Gly1045Arg(p.G1045R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1839203:1839203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3026C>A
AA Mutation	p.Thr1009Lys(p.T1009K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1889309:1889309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2452G>T
AA Mutation	p.Asp818Tyr(p.D818Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1912024:1912024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1705C>G
AA Mutation	p.Arg569Gly(p.R569G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1792340:1792340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3401A>G
AA Mutation	p.Asn1134Ser(p.N1134S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1922697:1922697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs192615880
CDS Mutation	c.1072C>T
AA Mutation	p.Arg358Cys(p.R358C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000399161
Start	1943130:1943130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.357T>A
AA Mutation	p.Asp119Glu(p.D119E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399161
Start	1840837:1840837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2781A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399161
Start	1922674:1922674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1095G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399161
Start	1943148:1943148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.339C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399161
Start	1922821:1922821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.948G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000399161
Start	1979531:1979531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.79G>T
AA Mutation	p.Glu27Ter(p.E27*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000399161
Start	1912019:1912019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1709+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript