Variant #0000614959 (NC_000014.8:g.36988353_36988381del, NM_003317.3:c.188_216del (NKX2-1))
| Chromosome |
14 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.36988353_36988381del |
| DNA change (hg38) |
g.36519148_36519176del |
| Published as |
NKX2-1(NM_001079668.2):c.278_306del (p.(Ala93GlyfsTer336)) |
| ISCN |
- |
| DB-ID |
NKX2-1_000026 |
| 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_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2019-12-04 15:24:38 +01:00 (CET) |
| Date last edited |
2020-07-05 14:07:30 +02:00 (CEST) |

Variant on transcripts
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