Variant #0000167032 (NC_000001.10:g.171076966G>A, NM_001002294.2:c.472G>A (FMO3))
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Does not affect function |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.171076966G>A |
DNA change (hg38) |
g.171107825G>A |
Published as |
- |
ISCN |
- |
DB-ID |
FMO3_000008 See all 27 reported entries |
Variant remarks |
Sulindac: patients homozygous for E158K exhibit enhanced polyp regression in response to treatment |
Reference |
PubMed: Sachse 1999, PubMed: Hisamuddin 2004, PubMed: Hisamuddin 2005, PubMed: Soderberg 2012 |
ClinVar ID |
- |
dbSNP ID |
rs2266782 |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.37494 View details |
Owner |
Ornicha Prapapan |
Database submission license |
No license selected |
Created by |
Ornicha Prapapan |
Date created |
2013-02-21 16:34:07 +01:00 (CET) |
Date last edited |
2020-06-05 15:14:39 +02:00 (CEST) |

Variant on transcripts
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