Variant #0000521934 (NC_000004.11:g.15981529T>C, NC_000004.11(NM_006017.2):c.2490-2A>G (PROM1))
| Chromosome |
4 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.15981529T>C |
| DNA change (hg38) |
g.15979906T>C |
| Published as |
PROM1(NM_001145847.2):c.2463-2A>G |
| ISCN |
- |
| DB-ID |
PROM1_000015 See all 8 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) |
0.00013 View details |
| Owner |
VKGL-NL_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2020-06-16 12:42:56 +02:00 (CEST) |

Variant on transcripts
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