Variant #0000614033 (NC_000012.11:g.22089561G>A, NM_005691.2:c.48C>T (ABCC9))
Chromosome |
12 |
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.22089561G>A |
DNA change (hg38) |
g.21936627G>A |
Published as |
ABCC9(NM_020297.2):c.48C>T (p.N16=), ABCC9(NM_020297.4):c.48C>T (p.N16=) |
ISCN |
- |
DB-ID |
ABCC9_000172 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) |
7.0E-5 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 |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
|