The ClinGen Evidence Repository is an FDA-recognized human genetic variant database containing expert-curated assertions regarding variants' pathogenicity and supporting evidence summaries.
[Disclaimer]
- Gene obtained from curated document aligns with the Allele Registry but not with ClinVar data
- No CSPEC computer assertion could be determined for this classification!
Variant: NM_000329.3(RPE65):c.1501_1505del (p.Tyr501fs)
CA2573132570
1384701 (ClinVar)
Gene: RPE65
Condition: RPE65-related recessive retinopathy
Inheritance Mode: Autosomal recessive inheritance
UUID: cba8ee55-d302-4f0e-944f-ca137444be3e
HGVS expressions
NM_000329.3:c.1501_1505del
NM_000329.3(RPE65):c.1501_1505del (p.Tyr501fs)
NC_000001.11:g.68429875_68429879del
CM000663.2:g.68429875_68429879del
NC_000001.10:g.68895558_68895562del
CM000663.1:g.68895558_68895562del
NC_000001.9:g.68668146_68668150del
NG_008472.1:g.25083_25087del
NG_008472.2:g.25083_25087del
ENST00000262340.6:c.1501_1505del
ENST00000262340.5:c.1501_1505del
NM_000329.2:c.1501_1505del
Evidence submitted by expert panel
Approved on: 2024-04-22
Published on: 2024-04-22
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