Variant #0000561553 (NC_000017.10:g.41131677C>G, PTGES3L-AARSD1(NM_025267.3):c.-43G>C)
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.41131677C>G |
DNA change (hg38) |
g.42979660C>G |
Published as |
PTGES3L(NM_001261430.1):c.141G>C (p.Q47H), PTGES3L-AARSD1(NM_001136042.2):c.141G>C (p.Q47H) |
ISCN |
- |
DB-ID |
AARSD1_000009 |
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_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |

Variant on transcripts
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