Variant #0000915382 (NC_000020.10:g.44520261_44520263del, NM_001278535.1:c.-610_-608del (NEURL2))
| Chromosome |
20 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.44520261_44520263del |
| DNA change (hg38) |
- |
| Published as |
CTSA(NM_000308.2):c.85_87del (p.(Leu37del)), CTSA(NM_001127695.2):c.54_56delGCT (p.L19del), CTSA(NM_001127695.3):c.54_56delGCT (p.L19del) |
| ISCN |
- |
| DB-ID |
CTSA_000002 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_VUmc |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_VUmc |
| Date created |
2023-01-11 15:44:22 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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