Variant #0000726454 (NC_000017.10:g.42945648_42945652del, NC_000017.10(NM_004247.3):c.1058+3_1058+7del (EFTUD2))
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.42945648_42945652del |
DNA change (hg38) |
- |
Published as |
EFTUD2(NM_001142605.1):c.953+3_953+7del (p.?), EFTUD2(NM_001258353.1):c.1058+3_1058+7delAAGTA, EFTUD2(NM_001258353.2):c.1058+3_1058+7delAAGTA |
ISCN |
- |
DB-ID |
EFTUD2_000022 See all 4 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) |
0.00548 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2021-02-08 18:36:18 +01:00 (CET) |
Date last edited |
2022-05-09 15:24:52 +02:00 (CEST) |

Variant on transcripts
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