Variant #0001049080 (NC_000011.9:g.67258362C>A, NM_003977.2:c.891C>A (AIP))
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.67258362C>A |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
AIP_000027 |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs35665586 |
Origin |
Unknown |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00133 View details |
Owner |
MobiDetails |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
MobiDetails |
Date created |
2025-10-10 16:41:02 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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