Variant #0000925093 (NC_000010.10:g.100186994dup, NM_000195.3:c.972dup (HPS1))
Chromosome |
10 |
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.100186994dup |
DNA change (hg38) |
- |
Published as |
HPS1(NM_000195.5):c.972dupC (p.M325Hfs*128) |
ISCN |
- |
DB-ID |
HPS1_000026 See all 5 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) |
Retrieve |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2023-04-16 21:50:28 +02:00 (CEST) |
Date last edited |
2024-10-29 21:08:56 +01:00 (CET) |

Variant on transcripts
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