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 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-09-25 14:45:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Predict/SIFT     

Predicted     
FH NM_000143.3 -/. - c.268-22A>T r.(?) p.(?) - -


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