Variant #0001046579 (NC_000016.9:g.71772912G>A, NM_001030007.1:c.2210C>T (AP1G1))
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.71772912G>A |
DNA change (hg38) |
- |
Published as |
AP1G1(NM_001030007.2):c.2210C>T (p.T737M) |
ISCN |
- |
DB-ID |
AP1G1_000028 |
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) |
3.0E-5 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2025-07-08 13:22:38 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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