Variant #0000288298 (NC_000001.10:g.92946625G>C, NM_005263.3:c.319C>G (GFI1))

Chromosome 1
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.92946625G>C
DNA change (hg38) g.92481068G>C
Published as GFI1(NM_001127215.2):c.319C>G (p.P107A), GFI1(NM_005263.3):c.319C>G (p.P107A)
ISCN -
DB-ID GFI1_000025 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) 0.00225 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GFI1 NM_005263.3 -?/. - c.319C>G r.(?) p.(Pro107Ala)


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