Variant #0000693101 (NC_000022.10:g.18905934A>G, NM_016335.4:c.1322T>C (PRODH))
Chromosome |
22 |
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.18905934A>G |
DNA change (hg38) |
- |
Published as |
PRODH(NM_016335.4):c.1322T>C (p.L441P), PRODH(NM_016335.5):c.1322T>C (p.L441P), PRODH(NM_016335.6):c.1322T>C (p.(Leu441Pro), p.L441P) |
ISCN |
- |
DB-ID |
PRODH_000012 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) |
0.00521 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2020-09-15 15:50:26 +02:00 (CEST) |
Date last edited |
2025-05-05 21:14:00 +02:00 (CEST) |

Variant on transcripts
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