Variant #0000538917 (NC_000010.10:g.102770434G>A, NM_001195263.1:c.2212C>T (PDZD7))
| Chromosome |
10 |
| 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.102770434G>A |
| DNA change (hg38) |
g.101010677G>A |
| Published as |
PDZD7(NM_001195263.1):c.2212C>T (p.L738=) |
| ISCN |
- |
| DB-ID |
LZTS2_000016 |
| 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 |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2020-06-29 10:20:17 +02:00 (CEST) |

Variant on transcripts
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