Variant #0000007826 (NC_000023.10:-, LAMP2(NM_002294.2):c.865-2A>G)
Chromosome |
X |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
No mutant RNA was detected from the mutation, perhaps indicating that this defect triggered missense |
DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
Reference |
GenBank |
DB-ID |
LAMP2_00022 |
Frequency |
- |
Variant remarks |
Intron |
ClassClinical |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Qi Ming |
Database submission license |
No license selected |
Created by |
Qi Ming |

Variant on transcripts
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