Variant #0000018020 (NC_000001.10:g.171072929C>A, NM_001002294.2:c.136C>A (FMO3))
Individual ID |
00103143 |
Chromosome |
1 |
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.171072929C>A |
DNA change (hg38) |
g.171103788C>A |
Published as |
- |
ISCN |
- |
DB-ID |
FMO3_000046 |
Variant remarks |
Rare variant. 1/140 chromosomes in Koreans |
Reference |
PubMed: Park et al. 1999 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
no |
Frequency |
1/140 chromosomes |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Ornicha Prapapan |
Database submission license |
No license selected |
Created by |
Ornicha Prapapan |
Date created |
2013-05-13 14:08:46 +02:00 (CEST) |
Date last edited |
2017-04-05 10:54:58 +02:00 (CEST) |

Variant on transcripts
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