Variant #0001002012 (NC_000016.9:g.2042220G>A, NM_005262.2:c.*6191G>A (GFER))

Chromosome 16
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.2042220G>A
DNA change (hg38) -
Published as SYNGR3(NM_004209.5):c.337+8G>A (p.?)
ISCN -
DB-ID GFER_000022
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SYNGR3 NM_004209.5 -?/. - c.337+8G>A r.(=) p.(=)
GFER NM_005262.2 -?/. - c.*6191G>A r.(=) p.(=)


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