Variant #0000276731 (NC_000023.10:g.135291619G>A, NC_000023.10(NM_001159702.2):c.888+18G>A (FHL1))

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.135291619G>A
DNA change (hg38) g.136209460G>A
Published as FHL1(NM_001159704.1):c.689-411G>A
ISCN -
DB-ID FHL1_000046
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) 2.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FHL1 NM_001159702.2 -/. - c.888+18G>A r.(=) p.(=)
MAP7D3 NM_024597.3 -/. - c.*9066C>T r.(=) p.(=)


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