Variant #0000184163 (NC_000023.10:g.(148568630_148571844)_(148586884_?)inv, IDS(NM_000202.5):c.(?_-217)_(1006+1_1007-1)inv)
Individual ID |
00114407 |
Chromosome |
X |
Allele |
Parent #1 |
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.(148568630_148571844)_(148586884_?)inv |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
IDS_000082 See all 11 reported entries |
Variant remarks |
- |
Reference |
PubMed: Isogai 1998 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
De novo |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2009-11-28 19:57:45 +01:00 (CET) |
Date last edited |
2017-08-08 16:07:12 +02:00 (CEST) |

Variant on transcripts
Screenings
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