Variant #0000980682 (NC_000013.10:g.39263913G>A, NM_207361.4:c.2432G>A (FREM2))

Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.39263913G>A
DNA change (hg38) -
Published as FREM2(NM_207361.4):c.2432G>A (p.(Gly811Glu)), FREM2(NM_207361.5):c.2432G>A (p.G811E), FREM2(NM_207361.6):c.2432G>A (p.G811E)
ISCN -
DB-ID FREM2_000200 See all 3 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) 0.00018 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FREM2 NM_207361.4 ?/. - c.2432G>A r.(?) p.(Gly811Glu)


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