Variant #0000924291 (NC_000005.9:g.156895736C>A, NM_001037332.2:c.*75728C>A (CYFIP2))
Chromosome |
5 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.156895736C>A |
DNA change (hg38) |
- |
Published as |
NIPAL4(NM_001099287.1):c.527C>A (p.A176D), NIPAL4(NM_001099287.2):c.341C>A (p.A114D), NIPAL4(NM_001172292.1):c.470C>A (p.A157D) |
ISCN |
- |
DB-ID |
NIPAL4_000004 See all 5 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) |
0.00066 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2023-04-16 21:50:28 +02:00 (CEST) |
Date last edited |
2023-07-07 10:10:56 +02:00 (CEST) |

Variant on transcripts
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