Variant #0000150179 (NC_000007.13:g.(75544498_75583306)_(75615168_75615240)del, NC_000007.13(NM_000941.2):c.(-5+1_-4-1)_(1669+1_1670-1)del (POR))
Chromosome |
7 |
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.(75544498_75583306)_(75615168_75615240)del |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
POR_000070 See all 2 reported entries |
Variant remarks |
- |
Reference |
PubMed: FukamiĀ 2009 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
Julia Lopez |
Date created |
2016-12-15 19:35:13 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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