Variant #0000761540 (NC_000006.11:g.42689961C>A, NM_000322.4:c.112G>T (PRPH2))
| Chromosome |
6 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.42689961C>A |
| DNA change (hg38) |
g.42722223C>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
PRPH2_000287 See all 2 reported entries |
| Variant remarks |
ACMG PVS1, PM2 |
| Reference |
PubMed: Peeters 2021, Journal: Peeters 2021 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
LOVD |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Manon Peeters |
| Date created |
2021-04-06 12:57:06 +02:00 (CEST) |
| Date last edited |
2021-10-29 16:20:22 +02:00 (CEST) |

Variant on transcripts
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