Mutation

Primary Site >> Liver Cancer

Gene >> TENM4

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278550
Start	78669573:78669573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6772G>A
AA Mutation	p.Asp2258Asn(p.D2258N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000278550
Start	78676295:78676295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5353C>G
AA Mutation	p.His1785Asp(p.H1785D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000278550
Start	79064846:79064846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.385G>A
AA Mutation	p.Val129Met(p.V129M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000278550
Start	78903368:78903368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.649G>C
AA Mutation	p.Asp217His(p.D217H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000278550
Start	78658668:78658668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7700G>A
AA Mutation	p.Gly2567Asp(p.G2567D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000278550
Start	78903272:78903272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.745A>C
AA Mutation	p.Thr249Pro(p.T249P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000278550
Start	78669606:78669606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758333727
CDS Mutation	c.6739C>T
AA Mutation	p.Arg2247Trp(p.R2247W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000278550
Start	78658126:78658126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8242T>A
AA Mutation	p.Tyr2748Asn(p.Y2748N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000278550
Start	78676159:78676159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5489G>A
AA Mutation	p.Arg1830Gln(p.R1830Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000278550
Start	78708471:78708471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4099A>G
AA Mutation	p.Thr1367Ala(p.T1367A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278550
Start	78701768:78701768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201252316
CDS Mutation	c.4845C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278550
Start	78658262:78658262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8106G>C
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278550
Start	78676236:78676236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5412C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278550
Start	78726134:78726134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3495G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000278550
Start	78702172:78702172(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4441delC
AA Mutation	p.Leu1481CysfsTer56(p.L1481Cfs*56)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000278550
Start	78771106:78771106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2425A>T
AA Mutation	p.Arg809Ter(p.R809*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000278550
Start	78814392:78814392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1685C>A
AA Mutation	p.Ser562Ter(p.S562*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript