Variant #0000097022 (NC_000007.13:g.[6027030_6027251del;6027252_6945161inv])
| Individual ID |
00065192 |
| Chromosome |
7 |
| Allele |
Both (homozygous) |
| 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.[6027030_6027251del;6027252_6945161inv] |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
chr7_000449 |
| Variant remarks |
- |
| Reference |
PubMed: Vogt 2016, Journal: Vogt 2016 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Julia Vogt |
| Database submission license |
No license selected |
| Created by |
Julia Vogt |
| Date created |
2016-05-20 15:51:11 +02:00 (CEST) |
| Date last edited |
2019-07-24 16:56:19 +02:00 (CEST) |

Variant on transcripts
Screenings
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