Variant #0000914103 (NC_000013.10:g.39261590C>T, NM_207361.4:c.109C>T (FREM2))

Chromosome 13
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.39261590C>T
DNA change (hg38) -
Published as FREM2(NM_207361.5):c.109C>T (p.L37F), FREM2(NM_207361.6):c.109C>T (p.L37F)
ISCN -
DB-ID FREM2_000004 See all 2 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) 0.00103 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FREM2 NM_207361.4 -?/. - c.109C>T r.(?) p.(Leu37Phe)


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