Variant #0001015984 (NC_000023.10:g.129265781_129265783del, NC_000023.10(NM_004208.3):c.1449-5_1449-3del (AIFM1))

Chromosome X
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.129265781_129265783del
DNA change (hg38) -
Published as AIFM1(NM_001130847.3):c.*677-5_*677-3delCTT, AIFM1(NM_004208.4):c.1449-5_1449-3delCTT
ISCN -
DB-ID AIFM1_000013 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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AIFM1 NM_004208.3 -?/. - c.1449-5_1449-3del r.spl? p.?


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