Variant #0000618488 (NC_000022.10:g.21350272G>A, NM_006767.3:c.2090G>A (LZTR1))
| Chromosome |
22 |
| 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.21350272G>A |
| DNA change (hg38) |
g.20995983G>A |
| Published as |
LZTR1(NM_006767.3):c.2090G>A (p.(Arg697Gln)), LZTR1(NM_006767.4):c.2090G>A (p.R697Q) |
| ISCN |
- |
| DB-ID |
LZTR1_000122 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) |
3.0E-5 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2019-12-04 15:24:38 +01:00 (CET) |
| Date last edited |
2025-02-07 18:57:27 +01:00 (CET) |

Variant on transcripts
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