Variant #0000570738 (NC_000021.8:g.44589243C>T, NM_000394.2:c.34C>T (CRYAA))
Chromosome |
21 |
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.44589243C>T |
DNA change (hg38) |
g.43169133C>T |
Published as |
CRYAA(NM_000394.2):c.34C>T (p.(Arg12Cys)), CRYAA(NM_000394.4):c.34C>T (p.R12C) |
ISCN |
- |
DB-ID |
CRYAA_000002 See all 18 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_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
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
|