Variant #0000521217 (NC_000004.11:g.113568916_113568917del, NM_016648.2:c.1068_1069del (LARP7))
| Chromosome |
4 |
| 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.113568916_113568917del |
| DNA change (hg38) |
g.112647760_112647761del |
| Published as |
LARP7(NM_001267039.4):c.1068_1069delAA (p.R357Efs*3) |
| ISCN |
- |
| DB-ID |
LARP7_000029 |
| 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_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2025-10-24 10:59:00 +02:00 (CEST) |

Variant on transcripts
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