Variant #0000269963 (NC_000022.10:g.17690428C>A, NM_017424.2:c.140G>T (CECR1))
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.17690428C>A |
DNA change (hg38) |
g.17209538C>A |
Published as |
ADA2(NM_001282225.2):c.140G>T (p.(Gly47Val), p.G47V), ADA2(NM_001282226.1):c.140G>T (p.G47V) |
ISCN |
- |
DB-ID |
CECR1_000016 See all 5 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) |
4.0E-5 View details |
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 |
2025-05-05 21:14:00 +02:00 (CEST) |

Variant on transcripts
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