Variant #0000163461 (NC_000016.9:g.16315534C>T, NM_001171.5:c.(191G>A) (ABCC6))
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.16315534C>T |
DNA change (hg38) |
g.16221677C>T |
Published as |
- |
ISCN |
- |
DB-ID |
ABCC6_000415 See all 2 reported entries |
Variant remarks |
variant co-amplified from ABCC6P1 (scored as heterozygous) |
Reference |
PubMed: Pulkkinen 2001 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Artefact |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2017-03-04 15:54:24 +01:00 (CET) |
Date last edited |
2020-07-14 22:02:50 +02:00 (CEST) |

Variant on transcripts
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