Variant #0000614031 (NC_000012.11:g.22068629G>A, NM_005691.2:c.789C>T (ABCC9))
Chromosome |
12 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.22068629G>A |
DNA change (hg38) |
g.21915695G>A |
Published as |
ABCC9(NM_020297.2):c.789C>T (p.C263=) |
ISCN |
- |
DB-ID |
ABCC9_000156 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) |
0.00392 View details |
Owner |
VKGL-NL_Nijmegen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Nijmegen |
Date created |
2019-12-04 15:24:38 +01:00 (CET) |
Date last edited |
2020-07-02 14:21:27 +02:00 (CEST) |

Variant on transcripts
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