Variant #0000564898 (NC_000018.9:g.44140411C>G, NM_144612.6:c.2696G>C (LOXHD1))
| Chromosome |
18 |
| 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.44140411C>G |
| DNA change (hg38) |
g.46560448C>G |
| Published as |
LOXHD1(NM_001384474.1):c.2696G>C (p.(Arg899Pro)), LOXHD1(NM_144612.6):c.2696G>C (p.R899P), LOXHD1(NM_144612.7):c.2696G>C (p.R899P) |
| ISCN |
- |
| DB-ID |
LOXHD1_000052 See all 5 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) |
0.00017 View details |
| Owner |
VKGL-NL_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2025-05-05 21:14:00 +02:00 (CEST) |

Variant on transcripts
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