Mutation

Primary Site >> Liver Cancer

Gene >> SLIT2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000504154
Start	20589665:20589665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3110T>A
AA Mutation	p.Leu1037Gln(p.L1037Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000504154
Start	20524123:20524123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1384C>T
AA Mutation	p.Arg462Cys(p.R462C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000504154
Start	20253877:20253877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.62A>G
AA Mutation	p.Asn21Ser(p.N21S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000504154
Start	20523817:20523817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1188C>A
AA Mutation	p.His396Gln(p.H396Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000504154
Start	20510511:20510511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.931A>G
AA Mutation	p.Thr311Ala(p.T311A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000504154
Start	20617186:20617186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4124G>A
AA Mutation	p.Cys1375Tyr(p.C1375Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000504154
Start	20595824:20595824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs80248215
CDS Mutation	c.3310G>A
AA Mutation	p.Glu1104Lys(p.E1104K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000504154
Start	20596472:20596472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3378T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000504154
Start	20533599:20533599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1716T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000504154
Start	20596505:20596505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3411C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000504154
Start	20533626:20533626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756174540
CDS Mutation	c.1743A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000504154
Start	20532012:20532012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761101181
CDS Mutation	c.1642T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000504154
Start	20550878:20550879(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2542_2543delCT
AA Mutation	p.Leu848PhefsTer16(p.L848Ffs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000504154
Start	20488943:20488943(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.737delA
AA Mutation	p.Asn246MetfsTer2(p.N246Mfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000504154
Start	20486225:20486225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.565A>T
AA Mutation	p.Arg189Ter(p.R189*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000504154
Start	20617187:20617187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4125C>A
AA Mutation	p.Cys1375Ter(p.C1375*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript