Variant #0000132260 (NC_000012.11:g.53823329C>T, NM_020547.2:c.1060C>T (AMHR2))
| Chromosome |
12 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.53823329C>T |
| DNA change (hg38) |
g.53429545C>T |
| Published as |
L354F |
| ISCN |
- |
| DB-ID |
AMHR2_000003 See all 2 reported entries |
| Variant remarks |
cDNA expression cloning, near normal activation ID3/SMAD6 transcription |
| 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 13:35:21 +02:00 (CEST) |
| Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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