Variant #0000287507 (NC_000023.10:g.135288752C>T, FHL1(NM_001159702.2):c.156+5C>T)

Chromosome X
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.135288752C>T
DNA change (hg38) g.136206593C>T
Published as FHL1(NM_001159699.1):c.204+5C>T (p.?), FHL1(NM_001159704.1):c.156+5C>T
ISCN -
DB-ID FHL1_000037 See all 6 reported entries
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) 0.00144 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FHL1 NM_001159702.2 -/. - c.156+5C>T r.spl? p.?