Variant #0000555234 (NC_000015.9:g.67457698A>G, NM_005902.3:c.508A>G (SMAD3))
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.67457698A>G |
DNA change (hg38) |
g.67165360A>G |
Published as |
SMAD3(NM_001145102.1):c.193A>G (p.(Ile65Val)), SMAD3(NM_005902.3):c.508A>G (p.I170V), SMAD3(NM_005902.4):c.508A>G (p.I170V) |
ISCN |
- |
DB-ID |
SMAD3_000021 See all 4 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) |
0.03979 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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