Variant #0000542292 (NC_000011.9:g.108382899_108382900insAGA, NM_015065.2:c.3334_3335insTCT (EXPH5))
| Chromosome |
11 |
| 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.108382899_108382900insAGA |
| DNA change (hg38) |
g.108512172_108512173insAGA |
| Published as |
EXPH5(NM_015065.3):c.3334_3335insTCT (p.K1112delinsI*) |
| ISCN |
- |
| DB-ID |
EXPH5_000013 |
| 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 |
2020-08-06 14:59:34 +02:00 (CEST) |

Variant on transcripts
|