Variant #0000675772 (NC_000001.10:g.240370951_240370952insTTCTTCCCGGGGCAGGCATACCCCTTCCTCCCC, NM_020066.4:c.2839_2840insTTCTTCCCGGGGCAGGCATACCCCTTCCTCCCC (FMN2))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.240370951_240370952insTTCTTCCCGGGGCAGGCATACCCCTTCCTCCCC |
| DNA change (hg38) |
- |
| Published as |
FMN2(NM_001305424.1):c.2851_2852ins33 (p.P950_P951ins11) |
| ISCN |
- |
| DB-ID |
FMN2_000086 |
| 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) |
0.00066 View details |
| Owner |
VKGL-NL_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2020-08-06 14:59:34 +02:00 (CEST) |
| Date last edited |
2020-09-15 15:50:26 +02:00 (CEST) |

Variant on transcripts
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