Variant #0000342671 (NC_000007.13:g.99703901C>T, NM_004722.3:c.1012C>T (AP4M1))
| Chromosome |
7 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.99703901C>T |
| DNA change (hg38) |
g.100106278C>T |
| Published as |
AP4M1(NM_004722.3):c.1012C>T (p.R338*), AP4M1(NM_004722.4):c.1012C>T (p.(Arg338*)) |
| ISCN |
- |
| DB-ID |
AP4M1_000003 See all 5 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) |
4.0E-5 View details |
| Owner |
VKGL-NL_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2025-02-07 18:57:27 +01:00 (CET) |

Variant on transcripts
|