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LOVD - Variant listings for MYB

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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
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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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- NC_000006.11:g.135411228T>C - - - - MYB_00004
- NC_000006.11:g.135415208G>A - - - - MYB_00003
- NC_000006.11:g.135419018T>C - - - - MYB_00007
- NC_000006.11:g.135419688T>C - - - - MYB_00008
- NC_000006.11:g.135422296A>T - - - - MYB_00009
- NC_000006.11:g.135435501T>C - - - - MYB_00001
- NC_000006.11:g.135445448C>T - - - - MYB_00005
- NC_000006.11:g.135451564T>A - - - - MYB_00002
- NC_000006.11:g.135458071T>C - - - - MYB_00006
- NM_001130173.1:c.1886A>C - NP_001123645.1:p.Glu626Ala - - MYB_00010
- NM_001130173.1:c.1892G>A - NP_001123645.1:p.Gly631Glu - - MYB_00012
- NM_001130173.1:c.1991C>T - NP_001123645.1:p.Ser664Leu - - MYB_00011
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Legend: [ MYB 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. MYB DB-ID: Database IDentifier; When available, links to OMIM ID's are provided.

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