Variant #0000896076 (NC_000023.10:g.27765444_27765446dup, NM_001136533.1:c.432_434dup (DCAF8L2))
Chromosome |
X |
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.27765444_27765446dup |
DNA change (hg38) |
- |
Published as |
DCAF8L2(NM_001353448.2):c.432_434dupGGA (p.E147dup) |
ISCN |
- |
DB-ID |
DCAF8L2_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) |
Retrieve |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2022-11-01 13:41:49 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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