Variant #0000328902 (NC_000022.10:g.21212987_21212992dup, NM_058004.3:c.42_47dup (PI4KA))
Chromosome |
22 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.21212987_21212992dup |
DNA change (hg38) |
g.20858699_20858704dup |
Published as |
PI4KA(NM_058004.3):c.42_47dupAGGCGG (p.G17_G18dup), PI4KA(NM_058004.3):c.47_48insAGGCGG (p.(Gly15_Gly16dup)), PI4KA(NM_058004.4):c.42_47dupAGGCGG ... |
ISCN |
- |
DB-ID |
PI4KA_000013 See all 3 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_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2021-09-17 14:40:49 +02:00 (CEST) |

Variant on transcripts
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