Variant #0000508577 (NC_000001.10:g.92944346_92944351dup, NC_000001.10(NM_005263.3):c.925-10_925-5dup (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.92944346_92944351dup
DNA change (hg38) g.92478789_92478794dup
Published as GFI1(NM_001127215.1):c.925-5_925-4insCTCTCT (p.(=)), GFI1(NM_005263.3):c.925-10_925-5dupCTCTCT, GFI1(NM_005263.3):c.925-12_925-7dupCTCTCT, GFI1(NM...)
ISCN -
DB-ID GFI1_000015 See all 3 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:07:21 +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.925-10_925-5dup r.spl? p.?


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