Variant #0000573508 (NC_000023.10:g.129299528G>A, NM_004208.3:c.103C>T (AIFM1))

Chromosome X
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.129299528G>A
DNA change (hg38) g.130165554G>A
Published as AIFM1(NM_001130847.3):c.103C>T (p.P35S, p.(Pro35Ser)), AIFM1(NM_001130847.4):c.103C>T (p.P35S)
ISCN -
DB-ID AIFM1_000026 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) 0.00129 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AIFM1 NM_004208.3 -/. - c.103C>T r.(?) p.(Pro35Ser)


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