Variant #0000323620 (NC_000014.8:g.24568362T>G, NRL(NM_006177.3):c.-14661A>C)
Chromosome |
14 |
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.24568362T>G |
DNA change (hg38) |
g.24099153T>G |
Published as |
PCK2(NM_001018073.1):c.769T>G (p.(Ser257Ala)) |
ISCN |
- |
DB-ID |
PCK2_000002 |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
0 |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Variant not found in online data sets |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |

Variant on transcripts
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