Variant #0000615398 (NC_000015.9:g.55724734G>A, NM_130810.3:c.1114C>T (DYX1C1))
| Chromosome |
15 |
| 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.55724734G>A |
| DNA change (hg38) |
g.55432536G>A |
| Published as |
DNAAF4(NM_130810.4):c.1114C>T (p.R372C) |
| ISCN |
- |
| DB-ID |
CCPG1_000007 |
| 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 View details |
| Owner |
VKGL-NL_VUmc |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_VUmc |
| Date created |
2019-12-04 15:24:38 +01:00 (CET) |
| Date last edited |
2020-07-06 15:03:26 +02:00 (CEST) |

Variant on transcripts
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