Variant #0000550871 (NC_000013.10:g.48571092_48571093del, NM_003850.2:c.160_161del (SUCLA2))
| Chromosome |
13 |
| 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.48571092_48571093del |
| DNA change (hg38) |
g.47996957_47996958del |
| Published as |
SUCLA2(NM_003850.2):c.160_161delTC (p.S54Tfs*3) |
| ISCN |
- |
| DB-ID |
SUCLA2_000015 |
| 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_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2020-07-03 16:56:01 +02:00 (CEST) |

Variant on transcripts
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