Variant #0000551319 (NC_000014.8:g.105173884_105173889del, NM_022489.3:c.1280_1285del (INF2))

Chromosome 14
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.105173884_105173889del
DNA change (hg38) g.104707547_104707552del
Published as INF2(NM_022489.3):c.1280_1285delCACCCC (p.P427_P428del), INF2(NM_022489.4):c.1280_1285delCACCCC (p.P427_P428del)
ISCN -
DB-ID INF2_000017 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) 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 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
INF2 NM_022489.3 -/. - c.1280_1285del r.(?) p.(Pro427_Pro428del)


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