Variant #0000436122 (NC_000023.10:g.135290014G>T, NM_001159702.2:c.395G>T (FHL1))
| Chromosome |
X |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.135290014G>T |
| DNA change (hg38) |
g.136207855G>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
FHL1_000014 See all 3 reported entries |
| Variant remarks |
expression cloning COS-7 and C2C12 cells gives dense large inclusions (mostly adjacent to nucleus) |
| Reference |
PubMed: Schessl 2008, OMIM:var0005 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2009-09-11 20:47:21 +02:00 (CEST) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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