Variant #0000537734 (NC_000009.11:g.14868740_14868749del, NC_000009.11(NM_144966.5):c.227_234+2del (FREM1))

Chromosome 9
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.14868740_14868749del
DNA change (hg38) g.14868742_14868751del
Published as FREM1(NM_144966.7):c.227_234+2delCTCCACAGGT
ISCN -
DB-ID FREM1_000179
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 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FREM1 NM_144966.5 +/. - c.227_234+2del r.spl? p.?


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