Variant #0000571615 (NC_000022.10:g.26849247G>A, NM_022081.5:c.2079C>T (HPS4))
| Chromosome |
22 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.26849247G>A |
| DNA change (hg38) |
g.26453281G>A |
| Published as |
HPS4(NM_001349903.2):c.1837C>T (p.R613W), HPS4(NM_022081.5):c.2079C>T (p.S693=) |
| ISCN |
- |
| DB-ID |
HPS4_000029 See all 2 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) |
0.00447 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 |
2022-05-09 15:51:19 +02:00 (CEST) |

Variant on transcripts
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