Variant #0000555195 (NC_000015.9:g.66995716C>T, NM_005585.4:c.120C>T (SMAD6))
Chromosome |
15 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.66995716C>T |
DNA change (hg38) |
g.66703378C>T |
Published as |
SMAD6(NM_005585.4):c.120C>T (p.G40=), SMAD6(NM_005585.5):c.120C>T (p.(Gly40=)) |
ISCN |
- |
DB-ID |
SMAD6_000022 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) |
0.03639 View details |
Owner |
VKGL-NL_Nijmegen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Nijmegen |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2025-05-05 21:14:00 +02:00 (CEST) |

Variant on transcripts
|