Variant #0001048388 (NC_000001.10:g.241677035T>A, NC_000001.10(NM_000143.3):c.268-22A>T (FH))
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.241677035T>A |
DNA change (hg38) |
- |
Published as |
- |
ISCN |
- |
DB-ID |
FH_000160 See all 5 reported entries |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs2275162 |
Origin |
Unknown |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.03413 View details |
Owner |
MobiDetails |
Database submission license |
Creative Commons Attribution 4.0 International |
Created by |
MobiDetails |
Date created |
2025-09-25 14:45:01 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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