Variant #0000000148 (NC_000006.11:g.135451564T>A)
Individual ID |
00000020, 00000062, 00000066, 00000067, 00000142, 00000155, 00000190, 00000193, 00000200, 00000238, 00000261, 00000298, 00000320, 00000357, 00000403, 00000443, 00000482, 00000491, 00000500, 00000537, 00000546, 00000743, 00000764, 00000780, 00000809, 00000811, 00000849, 00000858, 00000906, 00000969, 00000984, 00000987, 00001002, 00001018, 00001021, 00001023, 00001029, 00001039, 00001053, 00001058, 00001212, 00001225, 00001237, 00001243, 00001252, 00001258, 00001280, 00001284, 00001323, 00001366, 00001409, 00001429, 00001449, 00001503, 00001564, 00001578, 00001673, 00001709, 00001720, 00001761, 00001768, 00001799, 00001839, 00001854, 00001891, 00001896, 00001912, 00001934, 00001970, 00002029, 00002031, 00002052, 00002067 |
Chromosome |
6 |
Allele |
Both (homozygous) |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
Substitution |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.135451564T>A |
Reference |
GenBank;dbSNP |
DB-ID |
MYB_000001 See all 3 reported entries |
Frequency |
- |
Variant remarks |
- |
ClassClinical |
Likely benign |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Qi Ming |
Database submission license |
No license selected |
Created by |
Qi Ming |

Variant on transcripts
Screenings
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