Variant #0000619673 (NC_000023.10:g.50350727dup, NM_020717.3:c.3415dup (SHROOM4))
| Chromosome |
X |
| 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.50350727dup |
| DNA change (hg38) |
g.50607727dup |
| Published as |
SHROOM4(NM_020717.3):c.3415dup (p.(Glu1139Glyfs*39)), SHROOM4(NM_020717.3):c.3415dupG (p.E1139Gfs*39) |
| ISCN |
- |
| DB-ID |
SHROOM4_000041 See all 3 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_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2019-12-04 15:24:38 +01:00 (CET) |
| Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
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