Variant #0000140585 (NC_000019.9:g.8669873T>C, NC_000019.9(NM_030957.2):c.435+24A>G (ADAMTS10))
Individual ID |
00088066 |
Chromosome |
19 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Does not affect function |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.8669873T>C |
DNA change (hg38) |
g.8604988= |
Published as |
- |
ISCN |
- |
DB-ID |
ADAMTS10_000005 See all 2 reported entries |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs7260282 |
Origin |
Unknown |
Segregation |
- |
Frequency |
Global MAF T=0.1786/388 |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.77913 View details |
Owner |
Andreas Laner |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
Andreas Laner |
Date created |
2014-10-13 12:09:00 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
Screenings
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