Variant #0000508909 (NC_000002.11:g.109513572T>G, NM_022336.3:c.1138A>C (EDAR))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.109513572T>G |
| DNA change (hg38) |
g.108897116T>G |
| Published as |
EDAR(NM_022336.3):c.1138A>C (p.S380R, p.(Ser380Arg)) |
| ISCN |
- |
| DB-ID |
EDAR_000011 See all 3 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) |
0.00173 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2019-12-04 14:54:23 +01:00 (CET) |

Variant on transcripts
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