Variant #0000640792 (NC_000008.10:g.72229893_72229894del, EYA1(NM_000503.4):c.450_451del)
Individual ID |
00283900 |
Chromosome |
8 |
Allele |
Parent #1 |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.72229893_72229894del |
DNA change (hg38) |
g.71317658_71317659del |
Published as |
- |
ISCN |
- |
DB-ID |
EYA1_000199 |
Variant remarks |
- |
Reference |
MORL Deafness Variation Database, PubMed: Orten 2008 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
0 |
Methylation |
- |
Average frequency (large NGS studies) |
Variant not found in online data sets |
Owner |
Global Variome, with Curator vacancy |

Variant on transcripts
Screenings
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