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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 ASNS:

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
ENSG00000070669	ASNS	0	0	6	ENSG00000070669	ENST00000462436		asparagine synthetase (glutamine-hydrolyzing) [Source:HGNC Symbol;Acc:753]	7	97481430	97501854	-1	q21.3	97484303	97487691	ASNS	ASNS-013	HGNC Symbol	HGNC transcript name	17	38.42	protein_coding	retained_intron	ensembl_hava	havana	KNOWN	KNOWN	440	753	ASNS		27506

MSeqDR Master Exome Data Set M1: 216 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	97481466	C	A	ENST00000175506	ENSG00000070669	97481430	97501854	ENSP00000175506	ASNS	-1	ASNS_HUMAN	-	-	3'_UTR	rs75198492	0.0671	-	-	-	-	-	het	6
2	7	97481466	C	A	ENST00000175506	ENSG00000070669	97481430	97501854	ENSP00000175506	ASNS	-1	ASNS_HUMAN	-	-	3'_UTR	rs75198492	0.0671	-	-	-	-	-	hom	1
3	7	97481466	C	A	ENST00000394308	ENSG00000070669	97481430	97501854	ENSP00000377845	ASNS	-1	ASNS_HUMAN	-	-	3'_UTR	rs75198492	0.0671	-	-	-	-	-	het	6
4	7	97481466	C	A	ENST00000394308	ENSG00000070669	97481430	97501854	ENSP00000377845	ASNS	-1	ASNS_HUMAN	-	-	3'_UTR	rs75198492	0.0671	-	-	-	-	-	hom	1
5	7	97481466	C	A	ENST00000394309	ENSG00000070669	97481430	97501854	ENSP00000377846	ASNS	-1	ASNS_HUMAN	-	-	3'_UTR	rs75198492	0.0671	-	-	-	-	-	het	6
6	7	97481466	C	A	ENST00000394309	ENSG00000070669	97481430	97501854	ENSP00000377846	ASNS	-1	ASNS_HUMAN	-	-	3'_UTR	rs75198492	0.0671	-	-	-	-	-	hom	1
7	7	97481466	C	A	ENST00000422745	ENSG00000070669	97481430	97501854	ENSP00000414901	ASNS	-1	ASNS_HUMAN	-	-	3'_UTR	rs75198492	0.0671	-	-	-	-	-	het	6
8	7	97481466	C	A	ENST00000422745	ENSG00000070669	97481430	97501854	ENSP00000414901	ASNS	-1	ASNS_HUMAN	-	-	3'_UTR	rs75198492	0.0671	-	-	-	-	-	hom	1
9	7	97481466	C	A	ENST00000437628	ENSG00000070669	97481430	97501854	ENSP00000414379	ASNS	-1	ASNS_HUMAN	-	-	3'_UTR	rs75198492	0.0671	-	-	-	-	-	het	6
10	7	97481466	C	A	ENST00000437628	ENSG00000070669	97481430	97501854	ENSP00000414379	ASNS	-1	ASNS_HUMAN	-	-	3'_UTR	rs75198492	0.0671	-	-	-	-	-	hom	1
11	7	97481466	C	A	ENST00000454046	ENSG00000070669	97481430	97501854	ENSP00000401651	ASNS	-1	-	-	-	3'_UTR	rs75198492	0.0671	-	-	-	-	-	het	6
12	7	97481466	C	A	ENST00000454046	ENSG00000070669	97481430	97501854	ENSP00000401651	ASNS	-1	-	-	-	3'_UTR	rs75198492	0.0671	-	-	-	-	-	hom	1
13	7	97481466	C	A	ENST00000455086	ENSG00000070669	97481430	97501854	ENSP00000408472	ASNS	-1	ASNS_HUMAN	-	-	3'_UTR	rs75198492	0.0671	-	-	-	-	-	het	6
14	7	97481466	C	A	ENST00000455086	ENSG00000070669	97481430	97501854	ENSP00000408472	ASNS	-1	ASNS_HUMAN	-	-	3'_UTR	rs75198492	0.0671	-	-	-	-	-	hom	1
15	7	97481491	T	G	ENST00000175506	ENSG00000070669	97481430	97501854	ENSP00000175506	ASNS	-1	ASNS_HUMAN	-	-	3'_UTR	rs115270247	0.0798	-	-	-	-	-	het	7
16	7	97481491	T	G	ENST00000394308	ENSG00000070669	97481430	97501854	ENSP00000377845	ASNS	-1	ASNS_HUMAN	-	-	3'_UTR	rs115270247	0.0798	-	-	-	-	-	het	7
17	7	97481491	T	G	ENST00000394309	ENSG00000070669	97481430	97501854	ENSP00000377846	ASNS	-1	ASNS_HUMAN	-	-	3'_UTR	rs115270247	0.0798	-	-	-	-	-	het	7
18	7	97481491	T	G	ENST00000422745	ENSG00000070669	97481430	97501854	ENSP00000414901	ASNS	-1	ASNS_HUMAN	-	-	3'_UTR	rs115270247	0.0798	-	-	-	-	-	het	7
19	7	97481491	T	G	ENST00000437628	ENSG00000070669	97481430	97501854	ENSP00000414379	ASNS	-1	ASNS_HUMAN	-	-	3'_UTR	rs115270247	0.0798	-	-	-	-	-	het	7
20	7	97481491	T	G	ENST00000454046	ENSG00000070669	97481430	97501854	ENSP00000401651	ASNS	-1	-	-	-	3'_UTR	rs115270247	0.0798	-	-	-	-	-	het	7

** 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,
**click here to view variant details for this gene in selected data set**,
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Transcripts and variants in the surrounding ASNS 7:97481430..97501854 region Gbrowse