Variant #0000335241 (NC_000023.10:g.114425889C>T, NC_000023.10(NM_020871.3):c.350-2956G>A (LRCH2))
| Chromosome |
X |
| 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.114425889C>T |
| DNA change (hg38) |
g.115191326C>T |
| Published as |
LRCH2(NM_001243963.1):c.350-2956G>A (p.(=)), RBMXL3(NM_001145346.1):c.1885C>T (p.R629C) |
| ISCN |
- |
| DB-ID |
LRCH2_000022 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) |
5.0E-5 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2020-09-15 15:50:26 +02:00 (CEST) |

Variant on transcripts
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