Variant #0000248667 (NC_000013.10:g.78477674A>G, NM_000115.3:c.552= (EDNRB))
| Chromosome |
13 |
| 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.78477674A>G |
| DNA change (hg38) |
g.77903539A>G |
| Published as |
EDNRB(NM_001201397.1):c.822T>C (p.S274=), EDNRB-AS1(NR_103853.1):n.1695-4153A>G |
| ISCN |
- |
| DB-ID |
EDNRB_000048 |
| 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) |
0.99585 View details |
| Owner |
VKGL-NL_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2023-11-27 17:27:23 +01:00 (CET) |

Variant on transcripts
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