Variant #0000565210 (NC_000018.9:g.59780367C>T, NM_176787.4:c.1434G>A (PIGN))
Chromosome |
18 |
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.59780367C>T |
DNA change (hg38) |
g.62113134C>T |
Published as |
PIGN(NM_012327.5):c.1434G>A (p.(=)), PIGN(NM_176787.4):c.1434G>A (p.K478=), PIGN(NM_176787.5):c.1434G>A (p.K478=) |
ISCN |
- |
DB-ID |
PIGN_000032 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_VUmc |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_VUmc |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2023-07-07 10:10:56 +02:00 (CEST) |

Variant on transcripts
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