Variant #0000001085 (NC_000011.9:g.5247905_5247906insA)
Individual ID |
00000025, 00000026, 00000032, 00000033, 00000034, 00000110, 00000230, 00000268, 00000291, 00000298, 00000412, 00000453, 00000457, 00000468, 00000513, 00000661, 00000662, 00000663, 00000676, 00000677, 00000679, 00000685, 00000688, 00000703, 00000709, 00000841, 00000898, 00000953, 00000965, 00000973, 00000984, 00000986, 00001165, 00001178, 00001205, 00001219, 00001221, 00001244, 00001245, 00001256, 00001258, 00001274, 00001280, 00001283, 00001285, 00001313, 00001314, 00001315, 00001319, 00001320, 00001327, 00001334, 00001339, 00001344, 00001347, 00001350, 00001387, 00001389, 00001397, 00001404, 00001411, 00001424, 00001437, 00001451, 00001456, 00001457, 00001465, 00001478, 00001497, 00001503, 00001572, 00001650, 00001652, 00001754, 00001759, 00001792, 00001802, 00001818, 00001873, 00001899, 00002026, 00002085 |
Chromosome |
11 |
Allele |
Parent #1 |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
Insertion |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.5247905_5247906insA |
Reference |
(OMIM 0328);dbSNP;Chen et al. |
DB-ID |
chr11_000313 |
Frequency |
- |
Variant remarks |
Codons 71/72 (+A) |
ClassClinical |
Pathogenic |
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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