Mutation

Primary Site >> Liver Cancer

Gene >> SYNE2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344113
Start	64027624:64027624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6545T>C
AA Mutation	p.Leu2182Ser(p.L2182S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344113
Start	64209556:64209556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.18518A>G
AA Mutation	p.Lys6173Arg(p.K6173R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000344113
Start	64024449:64024449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5830C>G
AA Mutation	p.Gln1944Glu(p.Q1944E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000344113
Start	64134114:64134114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.14560C>A
AA Mutation	p.Leu4854Met(p.L4854M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000344113
Start	64025391:64025391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6222G>A
AA Mutation	p.Met2074Ile(p.M2074I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000344113
Start	64087746:64087746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.11560A>C
AA Mutation	p.Ile3854Leu(p.I3854L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000344113
Start	64052747:64052747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8834G>A
AA Mutation	p.Cys2945Tyr(p.C2945Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000344113
Start	64051917:64051917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755099726
CDS Mutation	c.8004G>T
AA Mutation	p.Leu2668Phe(p.L2668F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000344113
Start	64141995:64141995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.15213G>T
AA Mutation	p.Trp5071Cys(p.W5071C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000344113
Start	64162224:64162224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.16247T>C
AA Mutation	p.Met5416Thr(p.M5416T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344113
Start	64056042:64056042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9843C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344113
Start	63990452:63990452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2355A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344113
Start	64186456:64186456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.17589G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344113
Start	64129829:64129829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.14067G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344113
Start	64053324:64053324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9411C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000344113
Start	64126362:64126371(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.13591_13600delAAAAAATTGT
AA Mutation	p.Lys4531LeufsTer5(p.K4531Lfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000344113
Start	64031040:64031040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6904C>T
AA Mutation	p.Gln2302Ter(p.Q2302*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000344113
Start	64219381:64219381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.19762G>T
AA Mutation	p.Glu6588Ter(p.E6588*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript