Variant #0000541821 (NC_000011.9:g.102987322A>G, NM_001080463.1:c.645A>G (DYNC2H1))
Chromosome |
11 |
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.102987322A>G |
DNA change (hg38) |
g.103116593A>G |
Published as |
DYNC2H1(NM_001080463.1):c.645A>G (p.L215=) |
ISCN |
- |
DB-ID |
DYNC2H1_000133 See all 2 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) |
0.00415 View details |
Owner |
VKGL-NL_Nijmegen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Nijmegen |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2020-07-01 11:19:27 +02:00 (CEST) |

Variant on transcripts
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