Variant #0000890035 (NC_000011.9:g.63990889G>A, NM_031471.5:c.1917G>A (FERMT3))

Chromosome 11
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.63990889G>A
DNA change (hg38) -
Published as FERMT3(NM_031471.6):c.1917G>A (p.T639=), FERMT3(NM_178443.2):c.1929G>A (p.T643=)
ISCN -
DB-ID FERMT3_000019 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) 0.0043 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 2022-11-01 13:01:21 +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     
FERMT3 NM_031471.5 -?/. - c.1917G>A r.(?) p.(Thr639=)
TRPT1 NM_031472.3 -?/. - c.*459C>T r.(=) p.(=)
NUDT22 NM_032344.2 -?/. - c.-3029G>A r.(?) p.(=)


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