LOVD - Variant listings for FLT1

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12 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
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Re-site Hide Re-site column Descending
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Frequency Hide Frequency column Descending
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DB-ID Hide DB-ID column Descending
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- NM_002019.4:c.1436+3896C>T - - - - FLT1_00004
- NM_002019.4:c.1437-4369G>A - - - - FLT1_00008
- NM_002019.4:c.1437-7030T>C - - - - FLT1_00001
- NM_002019.4:c.1551+3528G>A - - - - FLT1_00007
- NM_002019.4:c.1552-2416C>T - - - - FLT1_00003
- NM_002019.4:c.2116+67G>T - - - - FLT1_00002
- NM_002019.4:c.2356-2906A>G - - - - FLT1_00006
- NM_002019.4:c.3175-535T>C - - - - FLT1_00005
- NM_002019.4:c.64+4948C>T - - - - FLT1_00012
- NM_002019.4:c.65-2598A>G - - - - FLT1_00009
- NM_002019.4:c.65-4098T>C - - - - FLT1_00010
- NM_002019.4:c.65-8030G>T - - - - FLT1_00011
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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. FLT1 DB-ID: Database IDentifier; When available, links to OMIM ID's are provided.