Variant #0000000146 (NC_000006.11:g.135427817G>A)
Individual ID |
00000015, 00000020, 00000062, 00000067, 00000142, 00000155, 00000187, 00000190, 00000255, 00000257, 00000261, 00000294, 00000297, 00000357, 00000390, 00000416, 00000427, 00000447, 00000481, 00000537, 00000546, 00000619, 00000676, 00000743, 00000809, 00000811, 00000829, 00000849, 00000858, 00000865, 00000877, 00000882, 00000886, 00000906, 00000919, 00000972, 00000984, 00001002, 00001021, 00001023, 00001027, 00001029, 00001053, 00001058, 00001084, 00001096, 00001144, 00001155, 00001203, 00001210, 00001212, 00001220, 00001225, 00001237, 00001252, 00001256, 00001258, 00001284, 00001296, 00001323, 00001335, 00001356, 00001366, 00001399, 00001409, 00001429, 00001440, 00001503, 00001510, 00001642, 00001652, 00001673, 00001709, 00001720, 00001751, 00001761, 00001768, 00001777, 00001797, 00001833, 00001839, 00001840, 00001912, 00001934, 00001987 |
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.135427817G>A |
Reference |
GenBank;dbSNP |
DB-ID |
HBS1L_000006 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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