Variant #0000606004 (NC_000001.10:g.92944348_92944351dup, NC_000001.10(NM_005263.3):c.925-8_925-5dup (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.92944348_92944351dup
DNA change (hg38) g.92478791_92478794dup
Published as GFI1(NM_001127215.1):c.925-7_925-6insCTCT (p.(=)), GFI1(NM_001127215.2):c.925-10_925-7dupCTCT, GFI1(NM_005263.3):c.925-10_925-7dupCTCT, GFI1(NM_00...)
ISCN -
DB-ID GFI1_000034 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +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.925-8_925-5dup r.spl? p.?


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