Variant #0000140014 (NC_000016.9:g.16308351G>A, NC_000016.9(NM_001171.5):c.475-45C>T (ABCC6))
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.16308351G>A |
DNA change (hg38) |
g.16214494G>A |
Published as |
- |
ISCN |
- |
DB-ID |
ABCC6_000224 See all 2 reported entries |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs2239319 |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.05747 View details |
Owner |
Tim Hefferon |
Database submission license |
No license selected |
Created by |
Tim Hefferon |
Date created |
2013-02-16 00:10:40 +01:00 (CET) |
Date last edited |
2021-09-09 14:48:34 +02:00 (CEST) |

Variant on transcripts
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