Variant #0000324400 (NC_000016.9:g.1034730A>C, NM_022773.2:c.-13750T>G (LMF1))
| Chromosome |
16 |
| 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.1034730A>C |
| DNA change (hg38) |
g.984730A>C |
| Published as |
SOX8(NM_014587.3):c.685A>C (p.(Thr229Pro)), SOX8(NM_014587.4):c.685A>C (p.T229P) |
| ISCN |
- |
| DB-ID |
SOX8_000002 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) |
Retrieve |
| 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 |
2021-02-08 18:36:18 +01:00 (CET) |

Variant on transcripts
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