Variant #0000807105 (NC_000016.9:g.16267140C>A, NC_000016.9(NM_001171.5):c.2787+1G>T (ABCC6))
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.16267140C>A |
DNA change (hg38) |
- |
Published as |
ABCC6(NM_001171.6):c.2787+1G>T, ABCC6(NM_001351800.1):c.2445+1G>T |
ISCN |
- |
DB-ID |
ABCC6_000344 See all 19 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_VUmc |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_VUmc |
Date created |
2021-09-17 14:40:49 +02:00 (CEST) |
Date last edited |
2025-02-07 18:57:27 +01:00 (CET) |

Variant on transcripts
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