Variant #0000298465 (NC_000015.9:g.44865000T>C, NM_025137.3:c.6224A>G (SPG11))
| Chromosome |
15 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.44865000T>C |
| DNA change (hg38) |
g.44572802T>C |
| Published as |
SPG11(NM_025137.3):c.6224A>G (p.N2075S), SPG11(NM_025137.4):c.6224A>G (p.N2075S, p.(Asn2075Ser)) |
| ISCN |
- |
| DB-ID |
SPG11_000046 See all 7 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) |
0.00297 View details |
| Owner |
VKGL-NL_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2025-05-05 21:14:00 +02:00 (CEST) |

Variant on transcripts
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