Variant #0000335203 (NC_000023.10:g.110987996_110987998dup, NM_001099922.2:c.2796_2798dup (ALG13))
| Chromosome |
X |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.110987996_110987998dup |
| DNA change (hg38) |
g.111744768_111744770dup |
| Published as |
ALG13(NM_001099922.2):c.2753_2754insACC (p.(Pro945dup)), ALG13(NM_001257231.1):c.2562_2564dupACC (p.P867dup), ALG13(NM_001257231.2):c.2562_2564dupA... |
| ISCN |
- |
| DB-ID |
ALG13_000020 See all 3 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2024-02-26 20:06:56 +01:00 (CET) |

Variant on transcripts
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