Variant #0000279084 (NC_000001.10:g.180243706C>A, NM_033343.3:c.1165C>A (LHX4))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.180243706C>A |
| DNA change (hg38) |
g.180274571C>A |
| Published as |
LHX4(NM_033343.3):c.1165C>A (p.(Pro389Thr)), LHX4(NM_033343.4):c.1165C>A (p.P389T) |
| ISCN |
- |
| DB-ID |
LHX4_000015 See all 2 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) |
0.00028 View details |
| Owner |
VKGL-NL_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2024-08-28 13:07:21 +02:00 (CEST) |

Variant on transcripts
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