LOVD - Variant listings for KDR

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4 entries
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Exon Hide Exon column Descending
Ascending

DNA change   Descending
Ascending

RNA change Hide RNA change column Descending
Ascending

Protein Hide Protein column Descending
Ascending

Re-site Hide Re-site column Descending
Ascending

Frequency Hide Frequency column Descending
Ascending

DB-ID Hide DB-ID column Descending
Ascending
- NM_002253.2:c.1255+402G>A - - - - KDR_00003
- NM_002253.2:c.2266+1263G>A - - - - KDR_00002
- NM_002253.2:c.2267-749T>C - - - - KDR_00001
07 NM_002253.2:c.889G>A NM_002253.2:c.889G>A NP_002244.1:p.V297I - - KDR_00004
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Legend: [ KDR 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. KDR DB-ID: Database IDentifier; When available, links to OMIM ID's are provided.