Variant #0000930652 (NC_000016.9:g.71807130dup, NM_001030007.1:c.467dup (AP1G1))
Chromosome |
16 |
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.71807130dup |
DNA change (hg38) |
- |
Published as |
AP1G1(NM_001030007.2):c.467dupA (p.A157Gfs*14) |
ISCN |
- |
DB-ID |
AP1G1_000014 |
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_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2023-07-07 10:10:56 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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