Variant #0000300735 (NC_000011.9:g.45957234G>A, NM_001101802.1:c.1738C>T (PHF21A))
| Chromosome |
11 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.45957234G>A |
| DNA change (hg38) |
g.45935683G>A |
| Published as |
PHF21A(NM_001101802.2):c.1738C>T (p.R580*), PHF21A(NM_001101802.3):c.1738C>T (p.R580*), PHF21A(NM_001352025.1):c.1741C>T (p.R581*) |
| ISCN |
- |
| DB-ID |
PHF21A_000002 See all 4 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_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2023-07-07 10:10:56 +02:00 (CEST) |

Variant on transcripts
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