Variant #0000261431 (NC_000007.13:g.33423365_33423368del, NM_198428.2:c.1877_1880del (BBS9))
Chromosome |
7 |
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.33423365_33423368del |
DNA change (hg38) |
g.33383753_33383756del |
Published as |
BBS9(NM_001348038.3):c.1604_1607delAACA (p.K535Rfs*22), BBS9(NM_198428.3):c.1877_1880delAACA (p.K626Rfs*22) |
ISCN |
- |
DB-ID |
BBS9_000065 See all 6 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 |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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