Variant #0000539588 (NC_000010.10:g.14977469C>T, NM_001033855.1:c.457G>A (DCLRE1C))
Chromosome |
10 |
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.14977469C>T |
DNA change (hg38) |
g.14935470C>T |
Published as |
DCLRE1C(NM_001033858.3):c.97G>A (p.G33R), DCLRE1C(NM_001289079.2):c.97G>A (p.G33R) |
ISCN |
- |
DB-ID |
DCLRE1C_000008 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) |
0.01043 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2025-07-08 13:22:38 +02:00 (CEST) |

Variant on transcripts
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