Variant #0000544656 (NC_000011.9:g.58919923_58919932dup, NM_001312909.1:c.782_791dup (FAM111A))
| Chromosome |
11 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.58919923_58919932dup |
| DNA change (hg38) |
g.59152450_59152459dup |
| Published as |
FAM111A(NM_001142519.1):c.782_791dup (p.(Phe264Leufs*7)), FAM111A(NM_001142520.2):c.782_791dupGCAGATACTT (p.F264Lfs*7), FAM111A(NM_022074.4):c.782_... |
| ISCN |
- |
| DB-ID |
FAM111A_000004 See all 3 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_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2023-11-27 17:27:23 +01:00 (CET) |

Variant on transcripts
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