Variant #0001015221 (NC_000015.9:g.66995657G>A, NM_005585.4:c.61G>A (SMAD6))
Chromosome |
15 |
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.66995657G>A |
DNA change (hg38) |
- |
Published as |
SMAD6(NM_005585.5):c.61G>A (p.(Asp21Asn), p.D21N) |
ISCN |
- |
DB-ID |
SMAD6_000019 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) |
0.00515 View details |
Owner |
VKGL-NL_VUmc |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_VUmc |
Date created |
2024-10-29 21:08:56 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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