Mutation

Primary Site >> Liver Cancer

Gene >> TDRD5

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000294848
Start	179669264:179669264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2558C>T
AA Mutation	p.Thr853Ile(p.T853I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000294848
Start	179592796:179592796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.181C>T
AA Mutation	p.Pro61Ser(p.P61S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000294848
Start	179662276:179662276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2333T>C
AA Mutation	p.Met778Thr(p.M778T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000294848
Start	179634460:179634460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1130A>T
AA Mutation	p.Gln377Leu(p.Q377L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000294848
Start	179593652:179593652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.425T>A
AA Mutation	p.Leu142Gln(p.L142Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000294848
Start	179592785:179592785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.170T>C
AA Mutation	p.Val57Ala(p.V57A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000294848
Start	179662195:179662195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2252T>C
AA Mutation	p.Met751Thr(p.M751T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000294848
Start	179640445:179640445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1800G>T
AA Mutation	p.Glu600Asp(p.E600D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000294848
Start	179662104:179662104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2161G>A
AA Mutation	p.Asp721Asn(p.D721N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294848
Start	179635834:179635834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1467G>C
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294848
Start	179690748:179690748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2751T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294848
Start	179663440:179663440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147178825
CDS Mutation	c.2436A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294848
Start	179662181:179662181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2238T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294848
Start	179640436:179640436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1791A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294848
Start	179630886:179630886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1092A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294848
Start	179592624:179592624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.9A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294848
Start	179593575:179593575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.348A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294848
Start	179593584:179593584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.357G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000294848
Start	179595765:179595765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.778A>T
AA Mutation	p.Lys260Ter(p.K260*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000294848
Start	179595787:179595787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.800C>G
AA Mutation	p.Ser267Ter(p.S267*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000294848
Start	179630792:179630793(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1005dupA
AA Mutation	p.Leu336IlefsTer14(p.L336Ifs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript