Variant #0000855994 (NC_000021.8:g.46924429_46924443del, NM_030582.3:c.3367_3372del (COL18A1))
| Chromosome |
21 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.46924429_46924443del |
| DNA change (hg38) |
- |
| Published as |
COL18A1(NM_130444.3):c.4072_4086delCCCCCAGGCCCCCCA (p.P1358_R1362del), COL18A1(NM_130445.2):c.2827_2832delCCCCCA (p.(Pro943_Pro944del)) |
| ISCN |
- |
| DB-ID |
COL18A1_000215 See all 4 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_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2022-05-09 15:47:41 +02:00 (CEST) |
| Date last edited |
2026-01-20 18:57:21 +01:00 (CET) |

Variant on transcripts
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