Variant #0000276723 (NC_000023.10:g.135288613_135288616del, FHL1(NM_001159702.2):c.22_25del)

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.135288613_135288616del
DNA change (hg38) g.136206454_136206457del
Published as FHL1(NM_001159704.1):c.22_25delCACT (p.H8Tfs*21)
ISCN -
DB-ID FHL1_000034
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FHL1 NM_001159702.2 -?/. - c.22_25del r.(?) p.(His8ThrfsTer21)