Variant #0000761551 (NC_000006.11:g.42690036G>A, NM_000322.4:c.37C>T (PRPH2))
| Chromosome |
6 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.42690036G>A |
| DNA change (hg38) |
g.42722298G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
PRPH2_000070 See all 4 reported entries |
| Variant remarks |
ACMG PM5, PP3; ACMG criteria not strong enough to label as pathogenic |
| Reference |
PubMed: Peeters 2021, Journal: Peeters 2021 |
| ClinVar ID |
- |
| dbSNP ID |
rs61754402 |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00044 View details |
| 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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