Variant #0000761493 (NC_000006.11:g.42689632del, NM_000322.4:c.441del (PRPH2))
Chromosome |
6 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
ACMG |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.42689632del |
DNA change (hg38) |
g.42721894del |
Published as |
- |
ISCN |
- |
DB-ID |
PRPH2_000002 See all 31 reported entries |
Variant remarks |
ACMG PVS1, PS4, PM1, PP1 |
Reference |
PubMed: Peeters 2021, Journal: Peeters 2021 |
ClinVar ID |
- |
dbSNP ID |
rs61755784 |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0 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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