Variant #0000260595 (NC_000020.10:g.43251514G>A, NM_000022.2:c.736C>T (ADA))
Chromosome |
20 |
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.43251514G>A |
DNA change (hg38) |
g.44622873G>A |
Published as |
ADA(NM_000022.2):c.736C>T (p.Q246*), ADA(NM_000022.4):c.736C>T (p.Q246*) |
ISCN |
- |
DB-ID |
ADA_000035 See all 2 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 |
2025-07-08 13:22:38 +02:00 (CEST) |

Variant on transcripts
|