LOVD - Variant listings for MYB

Warning Please note that this overview may not be complete, as variants with unknown effect to the phenotype are left out.

About this overview [Show]

7 entries
entries per page

Exon Hide Exon column Descending

DNA change   Descending

RNA change Hide RNA change column Descending

Protein Hide Protein column Descending

Re-site Hide Re-site column Descending

Frequency Hide Frequency column Descending

DB-ID Hide DB-ID column Descending
- 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.135445448C>T - - - - MYB_00005
- NC_000006.11:g.135451564T>A - - - - MYB_00002
- NC_000006.11:g.135458071T>C - - - - MYB_00006
1 - 7

Save Click here to save this list in a tab-delimited text file.

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.