Variant #0000441404 (NC_000017.10:g.39942822_39942823del, NC_000017.10(NM_002230.2):c.-9+19_-9+20del (JUP))
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Does not affect function |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.39942822_39942823del |
DNA change (hg38) |
g.41786570_41786571del |
Published as |
-9+17_-9+18del2 |
ISCN |
- |
DB-ID |
JUP_000036 |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs67537421 |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Paul van der Zwaag |
Database submission license |
No license selected |
Created by |
Paul van der Zwaag |
Date created |
2009-09-01 15:35:06 +02:00 (CEST) |
Date last edited |
2020-07-13 13:38:55 +02:00 (CEST) |

Variant on transcripts
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