Variant #0000925835 (NC_000014.8:g.105173748A>G, NM_022489.3:c.1144A>G (INF2))

Chromosome 14
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.105173748A>G
DNA change (hg38) -
Published as INF2(NM_022489.3):c.1144A>G (p.S382G), INF2(NM_022489.4):c.1144A>G (p.S382G)
ISCN -
DB-ID INF2_000066 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) 0.00054 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
INF2 NM_022489.3 -?/. - c.1144A>G r.(?) p.(Ser382Gly)


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