Variant #0001014362 (NC_000007.13:g.47870813_47870814del, NC_000007.13(NM_138295.3):c.6473+2_6473+3del (PKD1L1))
| Chromosome |
7 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.47870813_47870814del |
| DNA change (hg38) |
- |
| Published as |
PKD1L1(NM_138295.5):c.6473+2_6473+3del, PKD1L1(NM_138295.5):c.6473+2_6473+3delTG |
| ISCN |
- |
| DB-ID |
C7orf69_000138 See all 2 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 |
2024-10-29 21:08:56 +01:00 (CET) |
| Date last edited |
2025-05-05 21:14:00 +02:00 (CEST) |

Variant on transcripts
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