Variant #0000001471 (NC_000002.11:g.49210264G>A, NM_000145.3:c.566C>T (FSHR))
| Chromosome |
2 |
| Allele |
Both (homozygous) |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
pathogenic (recessive) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.49210264G>A |
| DNA change (hg38) |
g.48983125G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
FSHR_000002 See all 17 reported entries |
| Variant remarks |
in vitro functional analysis shows dramatic reduction of binding capacity and signal transduction of the variant receptor |
| Reference |
PubMed: Aittomaki 1995, OMIM:var0001 |
| ClinVar ID |
- |
| dbSNP ID |
rs121909658 |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00076 View details |
| Owner |
Anne Polvi |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Anne Polvi |
| Date created |
2012-08-23 16:32:11 +02:00 (CEST) |
| Date last edited |
2023-02-08 13:39:32 +01:00 (CET) |

Variant on transcripts
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