Variant #0000508590 (NC_000001.10:g.92948938C>T, NM_005263.3:c.107G>A (GFI1))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.92948938C>T
DNA change (hg38) g.92483381C>T
Published as GFI1(NM_001127215.1):c.107G>A (p.(Ser36Asn)), GFI1(NM_005263.3):c.107G>A (p.S36N)
ISCN -
DB-ID GFI1_000026 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) 0.03985 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GFI1 NM_005263.3 -/. - c.107G>A r.(?) p.(Ser36Asn)


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