Variant #0000531694 (NC_000007.13:g.21939007_21939008del, NM_001277115.1:c.13103_13104del (DNAH11))
| Chromosome |
7 |
| 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.21939007_21939008del |
| DNA change (hg38) |
g.21899389_21899390del |
| Published as |
DNAH11(NM_001277115.1):c.13103_13104delTT (p.L4368Hfs*30), DNAH11(NM_001277115.2):c.13103_13104del (p.(Leu4368Hisfs*30)), DNAH11(NM_001277115.2):c.... |
| ISCN |
- |
| DB-ID |
DNAH11_000129 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_VUmc |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_VUmc |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2025-11-01 13:22:20 +01:00 (CET) |

Variant on transcripts
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