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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

MSeqDR Central Portal

MSeqDR Data Summary for the Term FLNC:

Ensembl Gene ID	Associated Gene Name	LSDB Genes	LSDB Variants	clinVar hits	Ensembl Gene ID	Ensembl Transcript ID	Ensembl Protein ID	Description	Chr	Gene Start	Gene End	Strand	Band	Transcript Start bp	Transcript End bp	Associated Gene Name	Associated Transcript Name	Associated Gene DB	Associated Transcript DB	Transcript count	pct GC content	Gene Biotype	Transcript Biotype	Source Gene	Source Transcript	Status gene	Status transcript	EntrezGene ID	HGNC ID	HGNC Symbol	RefSeq mRNA	Seq region id
ENSG00000128591	FLNC	0	0	59	ENSG00000128591	ENST00000325888	ENSP00000327145	filamin C, gamma [Source:HGNC Symbol;Acc:3756]	7	128470431	128499328	1	q32.1	128470431	128499326	FLNC	FLNC-001	HGNC Symbol	HGNC transcript name	3	60.86	protein_coding	protein_coding	ensembl_hava	ensembl_hava	KNOWN	KNOWN	2318	3756	FLNC	NM_001458	27506

MSeqDR Master Exome Data Set M1: 363 entries from same gene

No.	Chr	Position	Reference	Variant	EnsemblTranscriptID	EnsemblGeneID	Gene_Start	Gene_End	EnsemblProteinID	Gene	strand	Uniprot	cChange	pChange	Nature	dbSNP	Freq	EVS	phastCons	SIFT	Polyphen	HGMD	type	samples
1	7	128470462	C	A	ENST00000325888	ENSG00000128591	128470431	128499328	ENSP00000327145	FLNC	1	FLNC_HUMAN	-	-	5'_UTR	rs2472290	1	-	lod=249:559	-	-	-	het	9
2	7	128470462	C	A	ENST00000325888	ENSG00000128591	128470431	128499328	ENSP00000327145	FLNC	1	FLNC_HUMAN	-	-	5'_UTR	rs2472290	1	-	lod=249:559	-	-	-	hom	585
3	7	128470482	G	A	ENST00000325888	ENSG00000128591	128470431	128499328	ENSP00000327145	FLNC	1	FLNC_HUMAN	-	-	5'_UTR	rs2639138	1	-	lod=249:559	-	-	-	hom	648
4	7	128470482	G	A	ENST00000346177	ENSG00000128591	128470431	128499328	ENSP00000344002	FLNC	1	FLNC_HUMAN	-	-	5'_UTR	rs2639138	1	-	lod=249:559	-	-	-	hom	648
5	7	128470485	C	G	ENST00000325888	ENSG00000128591	128470431	128499328	ENSP00000327145	FLNC	1	FLNC_HUMAN	-	-	5'_UTR	NA	-	-	lod=249:559	-	-	-	hom	1
6	7	128470485	C	G	ENST00000325888	ENSG00000128591	128470431	128499328	ENSP00000327145	FLNC	1	FLNC_HUMAN	-	-	5'_UTR	NA	-	-	lod=249:559	-	-	-	het	2
7	7	128470485	C	G	ENST00000346177	ENSG00000128591	128470431	128499328	ENSP00000344002	FLNC	1	FLNC_HUMAN	-	-	5'_UTR	NA	-	-	lod=249:559	-	-	-	hom	1
8	7	128470485	C	G	ENST00000346177	ENSG00000128591	128470431	128499328	ENSP00000344002	FLNC	1	FLNC_HUMAN	-	-	5'_UTR	NA	-	-	lod=249:559	-	-	-	het	2
9	7	128470493	A	G	ENST00000325888	ENSG00000128591	128470431	128499328	ENSP00000327145	FLNC	1	FLNC_HUMAN	-	-	5'_UTR	NA	-	-	lod=249:559	-	-	-	het	15
10	7	128470493	A	G	ENST00000346177	ENSG00000128591	128470431	128499328	ENSP00000344002	FLNC	1	FLNC_HUMAN	-	-	5'_UTR	NA	-	-	lod=249:559	-	-	-	het	15
11	7	128470610	G	A	ENST00000325888	ENSG00000128591	128470431	128499328	ENSP00000327145	FLNC	1	FLNC_HUMAN	-	-	5'_UTR	NA	-	-	-	-	-	-	het	5
12	7	128470610	G	A	ENST00000346177	ENSG00000128591	128470431	128499328	ENSP00000344002	FLNC	1	FLNC_HUMAN	-	-	5'_UTR	NA	-	-	-	-	-	-	het	5
13	7	128470649	A	G	ENST00000325888	ENSG00000128591	128470431	128499328	ENSP00000327145	FLNC	1	FLNC_HUMAN	-	-	5'_UTR	NA	-	-	-	-	-	-	het	1
14	7	128470649	A	G	ENST00000346177	ENSG00000128591	128470431	128499328	ENSP00000344002	FLNC	1	FLNC_HUMAN	-	-	5'_UTR	NA	-	-	-	-	-	-	het	1
15	7	128470680	G	T	ENST00000325888	ENSG00000128591	128470431	128499328	ENSP00000327145	FLNC	1	FLNC_HUMAN	-	-	5'_UTR	rs199842696	-	T=0/G=8268;T=64/G=3884;T=64/G=12152	lod=62:410	-	-	-	het	1
16	7	128470680	G	T	ENST00000346177	ENSG00000128591	128470431	128499328	ENSP00000344002	FLNC	1	FLNC_HUMAN	-	-	5'_UTR	rs199842696	-	T=0/G=8268;T=64/G=3884;T=64/G=12152	lod=62:410	-	-	-	het	1
17	7	128470838	C	T	ENST00000325888	ENSG00000128591	128470431	128499328	ENSP00000327145	FLNC	1	FLNC_HUMAN	c.147C>T	p.H49H	syn	rs3734972	0.1711	T=732/C=7868;T=487/C=3917;T=1219/C=11785	lod=1716:765	-	-	-	het	161
18	7	128470838	C	T	ENST00000325888	ENSG00000128591	128470431	128499328	ENSP00000327145	FLNC	1	FLNC_HUMAN	c.147C>T	p.H49H	syn	rs3734972	0.1711	T=732/C=7868;T=487/C=3917;T=1219/C=11785	lod=1716:765	-	-	-	hom	6
19	7	128470838	C	T	ENST00000346177	ENSG00000128591	128470431	128499328	ENSP00000344002	FLNC	1	FLNC_HUMAN	c.147C>T	p.H49H	syn	rs3734972	0.1711	T=732/C=7868;T=487/C=3917;T=1219/C=11785	lod=1716:765	-	-	-	het	161
20	7	128470838	C	T	ENST00000346177	ENSG00000128591	128470431	128499328	ENSP00000344002	FLNC	1	FLNC_HUMAN	c.147C>T	p.H49H	syn	rs3734972	0.1711	T=732/C=7868;T=487/C=3917;T=1219/C=11785	lod=1716:765	-	-	-	hom	6

** A friendly reminder: guest user can access up to first 20 entries per gene from MSeqDR Master Exome Data Set M1. To gain access to the full power of MSeqDR, please login, or register, then request access to data.

As MSeqDR registered user , your accessible protected data set after login:

Select a dataset from the above drop-down list,
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and click "Export" button to save as csv.

Transcripts and variants in the surrounding FLNC 7:128470431..128499328 region Gbrowse