Variant #0000949738 (NC_000011.9:g.63987487G>A, NM_031471.5:c.1204G>A (FERMT3))

Chromosome 11
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.63987487G>A
DNA change (hg38) -
Published as FERMT3(NM_031471.5):c.1204G>A (p.(Gly402Ser))
ISCN -
DB-ID FERMT3_000082
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FERMT3 NM_031471.5 ?/. - c.1204G>A r.(?) p.(Gly402Ser)
TRPT1 NM_031472.3 ?/. - c.*3861C>T r.(=) p.(=)


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