Variant #0000339229 (NC_000011.9:g.102991516A>G, NM_001080463.1:c.1233A>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.102991516A>G |
DNA change (hg38) |
g.103120787A>G |
Published as |
DYNC2H1(NM_001080463.1):c.1233A>G (p.Q411=) |
ISCN |
- |
DB-ID |
DYNC2H1_000022 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) |
0.01604 View details |
Owner |
VKGL-NL_Nijmegen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Nijmegen |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2020-07-01 11:19:32 +02:00 (CEST) |

Variant on transcripts
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