Variant #0000927261 (NC_000023.10:g.131214290G>A, NM_194277.2:c.910C>T (FRMD7))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.131214290G>A
DNA change (hg38) -
Published as FRMD7(NM_194277.2):c.910C>T (p.R304*), FRMD7(NM_194277.3):c.910C>T (p.R304*)
ISCN -
DB-ID FRMD7_000025 See all 5 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) 1.0E-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 2023-04-16 21:50:28 +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     
FRMD7 NM_194277.2 +/. - c.910C>T r.(?) p.(Arg304Ter)


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