Variant #0000335639 (NC_000023.10:g.135292017T>C, NC_000023.10(NM_001159702.2):c.889-13T>C (FHL1))
| Chromosome |
X |
| 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.135292017T>C |
| DNA change (hg38) |
g.136209858T>C |
| Published as |
FHL1(NM_001159699.1):c.737-13T>C (p.(=)), FHL1(NM_001159702.2):c.889-13T>C, FHL1(NM_001159704.1):c.689-13T>C, FHL1(NM_001159704.1):c.689-13_689-8de... |
| ISCN |
- |
| DB-ID |
FHL1_000051 See all 6 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 |
2020-03-23 16:13:27 +01:00 (CET) |

Variant on transcripts
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