Variant #0000341220 (NC_000005.9:g.156895736C>A, NM_001037332.2:c.*75728C>A (CYFIP2))
| Chromosome |
5 |
| 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.156895736C>A |
| DNA change (hg38) |
g.157468728C>A |
| 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_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2023-07-07 10:10:56 +02:00 (CEST) |

Variant on transcripts
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