View unique variants - The Globin Gene Server - Leiden Open Variation Database

About this overview [Show]

The variants below are all in the NOS3 database. In this view only variant fields are shown. Variants are listed only once, a number is present in the DNA change field when a variant has been reported more than once (in such cases fields other than the DNA change just belong to one entry and may differ for other entries).
Selecting and clicking a specific line will open a detailed view showing all variant entries, including patient and pathogenicity information.
At the bottom of this page a legend is provided with a short explanation of what each field contains.
For a more detailed description of each field, please see the NOS3 full legend here.

3 entries
entries per page

Exon

DNA change

RNA change

Protein

Re-site

Frequency

DB-ID


-	NM_000603.4:c.2113-408T>C	-	-	-	-	NOS3_00001
-	NM_000603.4:c.2685+113C>T	-	-	-	-	NOS3_00002
-	NM_000603.4:c.2984+228G>T	-	-	-	-	NOS3_00003

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Legend: [ NOS3 full legend ]
Sequence variations are described basically as recommended by the Ad-Hoc Committee for Mutation Nomenclature (AHCMN), with the recently suggested additions (den Dunnen JT and Antonarakis SE [2000], Hum.Mut. 15:7-12); for a summary see Nomenclature.
Exon: Exon numbering. DNA change: Variation at DNA-level. If present, "Full Details" will show you the the full-length entry. RNA change: Variation at RNA-level, (?) unknown but probably identical to DNA. Protein: Variation at protein level. Re-site: Variant creates (+) or destroys (-) a restriction enzyme recognition site. Frequency: Frequency if variant is non pathogenic. NOS3 DB-ID: Database IDentifier; When available, links to OMIM ID's are provided.

The Globin Gene Server

nitric oxide synthase 3 (endothelial cell) (NOS3)