Variant #0000558404 (NC_000016.9:g.51175677_51175685del, NM_002968.2:c.469_477del (SALL1))
| Chromosome |
16 |
| 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.51175677_51175685del |
| DNA change (hg38) |
g.51141766_51141774del |
| Published as |
SALL1(NM_001127892.1):c.178_186del (p.(Ser60_Ser62del)), SALL1(NM_001127892.2):c.178_186delAGCAGCAGC (p.S60_S62del), SALL1(NM_002968.2):c.469_477de... |
| ISCN |
- |
| DB-ID |
SALL1_000041 See all 4 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) |
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 |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
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