Variant #0000281024 (NC_000016.9:g.2035991C>T, NM_005262.2:c.580C>T (GFER))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.2035991C>T
DNA change (hg38) g.1985990C>T
Published as GFER(NM_005262.3):c.580C>T (p.R194C)
ISCN -
DB-ID GFER_000008 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) 4.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NOXO1 NM_001267721.1 +?/. - c.-4811G>A r.(?) p.(=)
SYNGR3 NM_004209.5 +?/. - c.-4113C>T r.(?) p.(=)
GFER NM_005262.2 +?/. - c.580C>T r.(?) p.(Arg194Cys)


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