Variant #0000914498 (NC_000016.9:g.2034876G>A, NM_005262.2:c.387G>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.2034876G>A
DNA change (hg38) -
Published as GFER(NM_005262.2):c.387G>A (p.(Met129Ile))
ISCN -
DB-ID GFER_000019
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 2023-01-11 15:44:22 +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     
NOXO1 NM_001267721.1 ?/. - c.-3696C>T r.(?) p.(=)
GFER NM_005262.2 ?/. - c.387G>A r.(?) p.(Met129Ile)


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