Variant #0001015187 (NC_000015.9:g.23892849G>T, NM_019066.4:c.41C>A (MAGEL2))
Chromosome |
15 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.23892849G>T |
DNA change (hg38) |
- |
Published as |
MAGEL2(NM_019066.4):c.41C>A (p.P14Q), MAGEL2(NM_019066.5):c.41C>A (p.P14Q) |
ISCN |
- |
DB-ID |
MAGEL2_000129 See all 2 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00053 View details |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2024-10-29 21:08:56 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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