Variant #0001022242 (NC_000023.10:g.129270665C>T, NM_004208.3:c.1117G>A (AIFM1))
| Chromosome |
X |
| 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.129270665C>T |
| DNA change (hg38) |
g.130136690C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
AIFM1_000039 See all 3 reported entries |
| Variant remarks |
in vitro analysis 293T cells mini-gene exon trapping assay: effect on RNA inclusion of intron sequences |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Tjakko van Ham |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2024-11-05 16:15:00 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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