Variant #0000334426 (NC_000023.10:g.64738006_64738008del, NM_031206.4:c.1791_1793del (LAS1L))
| 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.64738006_64738008del |
| DNA change (hg38) |
g.65518126_65518128del |
| Published as |
LAS1L(NM_001170649.1):c.1740_1742del (p.(Asp580del)), LAS1L(NM_031206.4):c.1791_1793delTGA (p.D597del), LAS1L(NM_031206.7):c.1791_1793delTGA (p.D5...) |
| ISCN |
- |
| DB-ID |
LAS1L_000011 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 |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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