Variant #0000930061 (NC_000012.11:g.22068591C>T, NC_000012.11(NM_005691.2):c.816+11G>A (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.22068591C>T |
| DNA change (hg38) |
- |
| Published as |
ABCC9(NM_001377273.1):c.816+11G>A, ABCC9(NM_020297.4):c.816+11G>A |
| ISCN |
- |
| DB-ID |
ABCC9_000154 See all 2 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) |
0.00013 View details |
| Owner |
VKGL-NL_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2023-07-07 10:10:56 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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