Variant #0000866718 (NC_000022.10:g.17690409G>A, NM_017424.2:c.159= (CECR1))
Chromosome |
22 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.17690409G>A |
DNA change (hg38) |
- |
Published as |
ADA2(NM_001282225.2):c.159C>T (p.N53=) |
ISCN |
- |
DB-ID |
CECR1_000030 See all 3 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) |
0.43376 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2022-05-09 16:01:56 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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