Variant #0000062820 (NC_000019.9:g.10883126C>G, NC_000019.9(NM_001005360.2):c.236-29C>G (DNM2))
Individual ID |
00035625 |
Chromosome |
19 |
Allele |
Parent #1 |
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.10883126C>G |
DNA change (hg38) |
g.10772450C>G |
Published as |
- |
ISCN |
- |
DB-ID |
DNM2_000027 |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs3826803 |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.55292 View details |
Owner |
Andreas Laner |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
Julia Lopez |
Date created |
2015-04-02 13:01:39 +02:00 (CEST) |
Date last edited |
2015-11-08 12:14:38 +01:00 (CET) |

Variant on transcripts
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