Variant #0001035986 (NC_000007.13:g.100273948G>A, NM_022574.4:c.*5394C>T (GIGYF1))

Chromosome 7
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.100273948G>A
DNA change (hg38) -
Published as GNB2(NM_005273.4):c.57+3G>A
ISCN -
DB-ID GIGYF1_000058
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) 0.00029 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2025-05-05 21:14:00 +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     
GNB2 NM_005273.3 -?/. - c.57+3G>A r.spl? p.?
GIGYF1 NM_022574.4 -?/. - c.*5394C>T r.(=) p.(=)


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