Variant #0000680437 (NC_000016.9:g.2036000G>A, NM_005262.2:c.589G>A (GFER))

Chromosome 16
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.2036000G>A
DNA change (hg38) -
Published as GFER(NM_005262.2):c.589G>A (p.D197N)
ISCN -
DB-ID GFER_000014
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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +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.-4820C>T r.(?) p.(=)
SYNGR3 NM_004209.5 ?/. - c.-4104G>A r.(?) p.(=)
GFER NM_005262.2 ?/. - c.589G>A r.(?) p.(Asp197Asn)


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