Variant #0000612712 (NC_000010.10:g.88441223G>A, NC_000010.10(NM_001080114.1):c.321+1309G>A (LDB3))
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.88441223G>A |
DNA change (hg38) |
g.86681466G>A |
Published as |
LDB3(NM_001080115.1):c.352G>A (p.(Val118Met)), LDB3(NM_001171610.2):c.352G>A (p.V118M), LDB3(NM_007078.2):c.352G>A (p.V118M) |
ISCN |
- |
DB-ID |
LDB3_000127 See all 6 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) |
0.0043 View details |
Owner |
VKGL-NL_Nijmegen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Nijmegen |
Date created |
2019-12-04 15:24:38 +01:00 (CET) |
Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
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