Variant #0000300735 (NC_000011.9:g.45957234G>A, PHF21A(NM_001101802.1):c.1738C>T)
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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