Variant #0000877960 (NC_000009.11:g.13121734A>C, NC_000009.11(NM_001378778.1):c.5231+4T>G (MPDZ))
| Chromosome |
9 |
| 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.13121734A>C |
| DNA change (hg38) |
g.13121735A>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
MPDZ_000047 See all 2 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs199870788 |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00093 View details |
| Owner |
MobiDetails |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
MobiDetails |
| Date created |
2022-09-10 08:04:01 +02:00 (CEST) |
| Date last edited |
2024-02-19 09:52:53 +01:00 (CET) |

Variant on transcripts
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