Variant #0000132261 (NC_000012.11:g.53819477T>A, NM_020547.2:c.626T>A (AMHR2))
| Chromosome |
12 |
| 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.53819477T>A |
| DNA change (hg38) |
g.53425693T>A |
| Published as |
I209N |
| ISCN |
- |
| DB-ID |
AMHR2_000002 See all 2 reported entries |
| Variant remarks |
cDNA expression cloning, absent activation ID3/SMAD6 transcription (dominant negative effect) |
| Reference |
PubMed: Li 2016, Journal: Li 2016 |
| 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 |
2016-10-14 13:38:50 +02:00 (CEST) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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