Variant #0001020343 (NC_000014.8:g.65544706T>C, NM_002382.4:c.220A>G (MAX))
| Chromosome |
14 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
ACMG |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.65544706T>C |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CHURC1-FNTB_000001 See all 2 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Richarda de Voer |
| Database submission license |
No license selected |
| Created by |
Richarda de Voer |
| Date created |
2025-01-10 19:19:09 +01:00 (CET) |
| Date last edited |
2025-01-13 16:42:41 +01:00 (CET) |

Variant on transcripts
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