Variant #0000609284 (NC_000004.11:g.71508402_71508403insAG, NM_031889.2:c.1259_1260insAG (ENAM))
Chromosome |
4 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.71508402_71508403insAG |
DNA change (hg38) |
g.70642685_70642686insAG |
Published as |
ENAM(NM_031889.3):c.1259_1260insAG (p.P422Vfs*27) |
ISCN |
- |
DB-ID |
ENAM_000008 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) |
0.00029 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-12-04 14:54:23 +01:00 (CET) |
Date last edited |
2020-06-16 13:14:01 +02:00 (CEST) |

Variant on transcripts
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