Variant #0000553444 (NC_000014.8:g.94844947C>T, NM_001127701.1:c.1096G>A (SERPINA1))
Chromosome |
14 |
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.94844947C>T |
DNA change (hg38) |
g.94378610C>T |
Published as |
SERPINA1(NM_000295.4):c.1096G>A (p.(Glu366Lys)), SERPINA1(NM_001127701.1):c.1096G>A (p.E366K), SERPINA1(NM_001127701.2):c.1096G>A (p.E366K) |
ISCN |
- |
DB-ID |
SERPINA1_000004 See all 10 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) |
0.01112 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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