Variant #0000929056 (NC_000005.9:g.176831232G>T, NM_000505.3:c.983C>A (F12))
Chromosome |
5 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.176831232G>T |
DNA change (hg38) |
g.177404231G>T |
Published as |
F12(NM_000505.3):c.983C>A (p.T328K), F12(NM_000505.4):c.983C>A (p.T328K) |
ISCN |
- |
DB-ID |
F12_000008 See all 38 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 |
2023-07-07 10:10:56 +02:00 (CEST) |
Date last edited |
2024-02-26 20:06:56 +01:00 (CET) |

Variant on transcripts
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