Variant #0000604950 (NC_000001.10:g.161192875_161192884del, NM_004106.1:c.*4142_*4151del (FCER1G))
Chromosome |
1 |
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.161192875_161192884del |
DNA change (hg38) |
g.161223085_161223094del |
Published as |
APOA2(NM_001643.1):c.53-15_53-6delTGTGTGTGTG, APOA2(NM_001643.2):c.53-15_53-6delTGTGTGTGTG |
ISCN |
- |
DB-ID |
APOA2_000009 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 |
2019-12-04 14:54:23 +01:00 (CET) |
Date last edited |
2024-08-28 13:07:21 +02:00 (CEST) |

Variant on transcripts
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