Variant #0000792228 (NC_000019.9:g.?, NM_015629.3:c.? (PRPF31))
Chromosome |
19 |
Allele |
Both (homozygous) |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.? |
DNA change (hg38) |
- |
Published as |
p.R372 |
ISCN |
- |
DB-ID |
NPHS1_000138 See all 111 reported entries |
Variant remarks |
- |
Reference |
PubMed: Tanackovic 2011 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
Owner |
LOVD |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
Julia Lopez |
Date created |
2021-08-02 20:37:33 +02:00 (CEST) |
Date last edited |
2024-02-09 15:16:32 +01:00 (CET) |
Variant on transcripts
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