Variant #0000327391 (NC_000002.11:g.152584331_152584345del, NM_001271208.1:c.169_183del (NEB))
Chromosome |
2 |
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.152584331_152584345del |
DNA change (hg38) |
g.151727817_151727831del |
Published as |
NEB(NM_001164507.1):c.169_183del (p.(Leu57_Ala61del)), NEB(NM_001271208.1):c.169_183delCTGGCACAGCCAGCA (p.L57_A61del) |
ISCN |
- |
DB-ID |
NEB_000496 |
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_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2024-04-19 20:20:39 +02:00 (CEST) |

Variant on transcripts
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