Variant #0000543974 (NC_000011.9:g.45957314_45957315del, NC_000011.9(NM_001101802.1):c.1682-4_1682-3del (PHF21A))
| Chromosome |
11 |
| 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.45957314_45957315del |
| DNA change (hg38) |
g.45935763_45935764del |
| Published as |
PHF21A(NM_001101802.1):c.1682-6_1682-5del (p.?), PHF21A(NM_016621.4):c.1544-4_1544-3delTT |
| ISCN |
- |
| DB-ID |
PHF21A_000004 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) |
Retrieve |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2025-02-07 18:57:27 +01:00 (CET) |

Variant on transcripts
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