Variant #0000245356 (NC_000001.10:g.155113074A>C, NM_018973.3:c.-268T>G (DPM3))
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.155113074A>C |
DNA change (hg38) |
g.155140598A>C |
Published as |
- |
ISCN |
- |
DB-ID |
DPM3_000002 |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs12745576 |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2010-04-16 20:05:12 +02:00 (CEST) |
Date last edited |
2018-01-14 21:40:42 +01:00 (CET) |

Variant on transcripts
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