Variant #0000017051 (NC_000001.10:g.46657769C>T, NC_000001.10(NM_001243766.1):c.1539+1G>A (POMGNT1))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic (recessive) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.46657769C>T |
| DNA change (hg38) |
g.46192097C>T |
| Published as |
IVS17+1G>A: Glu514read-through 526Stop/Leu472-His513del |
| ISCN |
- |
| DB-ID |
POMGNT1_000002 See all 49 reported entries |
| Variant remarks |
Finnish Major/Founder MDDGA3(MEB) variant, causes splice defect, either exon 18 skipping or intron 18 inclusion |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00063 View details |
| Owner |
Anne Polvi |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Anne Polvi |
| Date created |
2013-01-31 14:09:45 +01:00 (CET) |
| Date last edited |
2022-03-08 20:46:45 +01:00 (CET) |

Variant on transcripts
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